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