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