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