--- 
- 
  allele_string: G/A
  assembly_name: GRCh38
  colocated_variants: 
    - 
      allele_string: G/A
      end: 1647710
      frequencies: 
        A: 
          af: '0.0002'
          afr: 0
          amr: 0
          eas: 0
          eur: 0
          gnomadg: '6.564e-06'
          gnomadg_afr: 0
          gnomadg_ami: 0
          gnomadg_amr: 0
          gnomadg_asj: 0
          gnomadg_eas: 0
          gnomadg_fin: 0
          gnomadg_mid: 0
          gnomadg_nfe: 0
          gnomadg_remaining: 0
          gnomadg_sas: '0.0002069'
          sas: '0.001'
      id: rs543148494
      seq_region_name: 20
      start: 1647710
      strand: 1
  end: 1647710
  id: rs543148494
  input: rs543148494
  most_severe_consequence: non_coding_transcript_exon_variant
  seq_region_name: 20
  start: 1647710
  strand: 1
  transcript_consequences: 
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000216927
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000303415
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000344103
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000381580
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000381583
      variant_allele: A
    - 
      biotype: lncRNA
      cdna_end: 2033
      cdna_start: 2033
      consequence_terms: 
        - non_coding_transcript_exon_variant
      gene_id: ENSG00000237914
      gene_symbol: SIRPG-AS1
      gene_symbol_source: HGNC
      hgnc_id: HGNC:51229
      impact: MODIFIER
      strand: 1
      transcript_id: ENST00000456177
      variant_allele: A
    - 
      biotype: protein_coding
      consequence_terms: 
        - intron_variant
      gene_id: ENSG00000089012
      gene_symbol: SIRPG
      gene_symbol_source: HGNC
      hgnc_id: HGNC:15757
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000885694
      variant_allele: A