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