UBE2K
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
439703194rs9683743TGrs96837435.70E-05Pericardial fatHPOID:0001717|HPOID:0001658DOID:5844TintronGWASdb_trait
439704197rs652162GArs6521626.62E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
439752636rs4974948GTrs49749485.90E-05Pericardial fatHPOID:0001717|HPOID:0001658DOID:5844GintronGWASdb_trait
439769260rs7687557ACrs76875576.90E-05Pericardial fatHPOID:0001717|HPOID:0001658DOID:5844AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000078140.13 UBE2K 602846