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