{"clinical_significance":["likely benign","drug response","other"],"ambiguity":"N","minor_allele":null,"synonyms":["rs60361278","rs17879456","rs116940633","124020.0001","RCV000018394","VCV000633856","RCV000018393","VCV001703261","RCV000610614","RCV000018395","RCV000352637","VCV000016897","RCV000783648","RCV002280383","PA166154053"],"mappings":[{"seq_region_name":"10","location":"10:94781859-94781859","end":94781859,"coord_system":"chromosome","start":94781859,"assembly_name":"GRCh38","ancestral_allele":"G","allele_string":"G/A/C/T","strand":1}],"name":"rs4244285","MAF":null,"evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"var_class":"SNP","source":"Variants (including SNPs and indels) imported from dbSNP","most_severe_consequence":"synonymous_variant"}