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