[{"ambiguity":"R","source":"Variants (including SNPs and indels) imported from dbSNP","clinical_significance":["benign","risk factor"],"mappings":[{"strand":1,"ancestral_allele":"G","coord_system":"chromosome","start":230710048,"assembly_name":"GRCh38","allele_string":"A/G","location":"1:230710048-230710048","end":230710048,"seq_region_name":"1"}],"MAF":0.2949,"synonyms":["106150.0001","NM_000029.4:c.803T>C","NM_000029.3:c.803T>C","NP_000020.1:p.Met268Thr","VAR_007096","rs4714","rs3182295","rs386606420","rs17856353","rs61617185","PA166153539","RCV000405686","RCV000835695","RCV000019691","RCV000019692","RCV000019693","RCV000242838","VCV000018068"],"minor_allele":"A","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"most_severe_consequence":"missense_variant","name":"rs699","var_class":"SNP"}]