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