{"synonyms":["PA166153539","106150.0001","NM_000029.3:c.803T>C","NP_000020.1:p.Met268Thr","RCV000019691","RCV000242838","RCV000019692","RCV000405686","RCV000019693","VAR_007096","rs386606420","rs61617185","rs17856353","rs4714","rs3182295"],"most_severe_consequence":"missense_variant","MAF":0.294928,"source":"Variants (including SNPs and indels) imported from dbSNP","ambiguity":"R","var_class":"SNP","clinical_significance":["benign","risk factor"],"ancestral_allele":"G","name":"rs699","genotyping_chips":["Illumina_HumanOmni2.5","Illumina_HumanOmni1-Quad","Illumina_ExomeChip","Illumina_HumanHap650Y","Illumina_ImmunoChip","Illumina_Human660W-quad","Illumina_Human610_Quad","HumanOmniExpress","Illumina_1M-duo","Illumina_HumanHap550"],"evidence":["Frequency","HapMap","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"minor_allele":"A","mappings":[{"allele_string":"A/G","end":230845794,"assembly_name":"GRCh37","coord_system":"chromosome","start":230845794,"strand":1,"location":"1:230845794-230845794","seq_region_name":"1"}]}