--- 
MAF: '0.00765306'
ambiguity: W
evidence: 
  - Frequency
  - 1000Genomes
  - Cited
  - TOPMed
  - gnomAD
mappings: 
  - 
    allele_string: T/A
    ancestral_allele: T
    assembly_name: GRCh38
    coord_system: chromosome
    end: 92150243
    location: 7:92150243-92150243
    seq_region_name: 7
    start: 92150243
    strand: 1
minor_allele: A
most_severe_consequence: intron_variant
name: rs7
source: Variants (including SNPs and indels) imported from dbSNP
synonyms: 
  - NM_016224.4:c.*1165C>T
  - NM_016224.5:c.*1165C>G
  - NM_016224.4:c.*1165C>G
  - NM_016224.5:c.*1165C>T
var_class: SNP