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