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