---
MAF: '0.498234'
ambiguity: ~
evidence:
  - Frequency
  - 1000Genomes
  - Cited
  - Phenotype_or_Disease
  - TOPMed
  - gnomAD
mappings:
  -
    allele_string: GGG/GG
    ancestral_allele: GGG
    assembly_name: GRCh38
    coord_system: chromosome
    end: 63847714
    location: 3:63847712-63847714
    seq_region_name: 3
    start: 63847712
    strand: 1
minor_allele: GGG
most_severe_consequence: intron_variant
name: rs34196118
source: Variants (including SNPs and indels) imported from dbSNP
synonyms:
  - rs376599565
  - rs398082152
  - rs397989891
  - rs66618638
  - rs142449327
  - rs66618639
  - rs79633187
  - rs66618635
  - rs373618301
  - rs66618637
  - rs66618634
  - rs66618636
var_class: indel