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