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