{"minor_allele":null,"MAF":null,"name":"rs116035550","ancestral_allele":"G","ambiguity":"R","genotypes":[],"evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"var_class":"SNP","most_severe_consequence":"missense_variant","mappings":[{"seq_region_name":"11","start":212464,"assembly_name":"GRCh37","strand":1,"end":212464,"coord_system":"chromosome","allele_string":"G/A","location":"11:212464-212464"}],"source":"Variants (including SNPs and indels) imported from dbSNP","synonyms":["NP_068751.4:p.Glu340Gln","NM_001286134.1:c.1018G>C","NP_001273063.1:p.Glu340Gln","NM_021932.5:c.1018G>A","NM_001286134.1:c.1018G>A","NP_068751.4:p.Glu340Lys","NP_001273063.1:p.Glu340Lys","NM_021932.5:c.1018G>C"]}