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