[{"minor_allele":"A","ambiguity":"R","most_severe_consequence":"missense_variant","source":"Variants (including SNPs and indels) imported from dbSNP","mappings":[{"ancestral_allele":"G","coord_system":"chromosome","start":230845794,"assembly_name":"GRCh37","seq_region_name":"1","allele_string":"A/G","strand":1,"end":230845794,"location":"1:230845794-230845794"}],"var_class":"SNP","name":"rs699","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"MAF":0.294928,"synonyms":["PA166153539","rs17856353","rs61617185","rs386606420","rs4714","rs3182295","NM_001382817.1:c.803T>C","NM_000029.4:c.803T>C","NM_001382817.2:c.776T>C","NM_001384479.1:c.776T>C","NP_001371408.1:p.Met259Thr","NM_000029.3:c.803T>C","NP_001369746.2:p.Met259Thr","NM_001382817.3:c.776T>C","RCV000019691","RCV000242838","VCV000018068","RCV000019693","RCV000835695","RCV000019692","RCV000405686","RCV002259306","VAR_007096","106150.0001"],"clinical_significance":["benign","risk factor"]}]