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