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