[{"synonyms":["PA166153539","VAR_007096","NM_001384479.1:c.776T>C","NM_001382817.2:c.776T>C","NM_000029.4:c.803T>C","NP_001371408.1:p.Met259Thr","NM_001382817.3:c.776T>C","NM_000029.3:c.803T>C","NP_001369746.2:p.Met259Thr","NM_001382817.1:c.803T>C","106150.0001","RCV000242838","RCV000835695","RCV000405686","RCV002259306","RCV000019693","RCV000019691","VCV000018068","RCV000019692","rs4714","rs3182295","rs17856353","rs61617185","rs386606420"],"clinical_significance":["benign"],"minor_allele":null,"evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"ambiguity":"R","source":"Variants (including SNPs and indels) imported from dbSNP","mappings":[{"end":230710048,"start":230710048,"allele_string":"A/G","seq_region_name":"1","assembly_name":"GRCh38","strand":1,"coord_system":"chromosome","ancestral_allele":"G","location":"1:230710048-230710048"}],"var_class":"SNP","name":"rs699","MAF":null,"most_severe_consequence":"missense_variant"}]