[{"mappings":[{"start":230845794,"location":"1:230845794-230845794","seq_region_name":"1","ancestral_allele":"G","assembly_name":"GRCh37","strand":1,"allele_string":"A/G","end":230845794,"coord_system":"chromosome"}],"evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"minor_allele":"A","most_severe_consequence":"missense_variant","MAF":0.294928,"ambiguity":"R","name":"rs699","synonyms":["rs61617185","rs386606420","rs17856353","rs3182295","rs4714","106150.0001","RCV000019692","RCV000835695","RCV002259306","RCV000242838","RCV000019691","RCV000019693","VCV000018068","RCV000405686","VAR_007096","PA166153539","NM_001382817.3:c.776T>C","NM_001382817.2:c.776T>C","NP_001369746.2:p.Met259Thr","NM_001382817.1:c.803T>C","NM_000029.4:c.803T>C","NM_000029.3:c.803T>C","NP_001371408.1:p.Met259Thr","NM_001384479.1:c.776T>C"],"clinical_significance":["benign","risk factor"],"var_class":"SNP","source":"Variants (including SNPs and indels) imported from dbSNP"}]