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