---
MAF: '0.222527'
ambiguity: ~
evidence:
  - Frequency
  - 1000Genomes
  - TOPMed
  - gnomAD
mappings:
  -
    allele_string: G/-
    ancestral_allele: ~
    assembly_name: GRCh38
    coord_system: chromosome
    end: 152632937
    location: 5:152632937-152632937
    seq_region_name: 5
    start: 152632937
    strand: 1
minor_allele: "-"
most_severe_consequence: intron_variant
name: rs112345465
source: Variants (including SNPs and indels) imported from dbSNP
synonyms:
  - rs144156774
  - rs376614525
var_class: deletion