--- 
MAF: '0.103414'
ambiguity: W
evidence: 
  - Frequency
  - 1000Genomes
  - TOPMed
  - gnomAD
mappings: 
  - 
    allele_string: T/A
    ancestral_allele: T
    assembly_name: GRCh38
    coord_system: chromosome
    end: 154120318
    location: 2:154120318-154120318
    seq_region_name: 2
    start: 154120318
    strand: 1
minor_allele: A
most_severe_consequence: intron_variant
name: rs1364535
source: Variants (including SNPs and indels) imported from dbSNP
synonyms: []

var_class: SNP