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