{"synonyms":[],"ambiguity":"D","var_class":"SNP","most_severe_consequence":"intron_variant","evidence":["Frequency","1000Genomes","TOPMed","gnomAD"],"name":"rs6691927","minor_allele":null,"source":"Variants (including SNPs and indels) imported from dbSNP","MAF":null,"mappings":[{"seq_region_name":"1","coord_system":"chromosome","location":"1:1584002-1584002","allele_string":"A/G/T","strand":1,"start":1584002,"ancestral_allele":null,"assembly_name":"GRCh37","end":1584002}]}