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