{"most_severe_consequence":"missense_variant","MAF":null,"minor_allele":null,"evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"ambiguity":"V","mappings":[{"location":"11:212464-212464","end":212464,"start":212464,"strand":1,"coord_system":"chromosome","allele_string":"G/A/C","seq_region_name":"11","assembly_name":"GRCh37","ancestral_allele":"G"}],"var_class":"SNP","name":"rs116035550","source":"Variants (including SNPs and indels) imported from dbSNP","synonyms":[]}