--- MAF: ~ 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: ~ most_severe_consequence: intron_variant name: rs1364535 source: Variants (including SNPs and indels) imported from dbSNP synonyms: [] var_class: SNP