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