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