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