USP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
162903359rs9436221TCrs94362211.47E-11Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162903363rs9436222CGrs94362221.48E-11Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162903547rs9436223CTrs94362231.60E-11Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162904295rs12029068CTrs120290685.69E-12Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162904575rs9436661TGrs94366619.09E-11Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162905893rs10493322CTrs104933228.40E-12Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162906489rs638714GTrs6387148.44E-12Metabolite levelsHPOID:0001939DOID:655NAintronGWASdb_trait
162906537rs638305GTrs6383058.46E-12Metabolite levelsHPOID:0001939DOID:655AintronGWASdb_trait
162906728rs637723CTrs6377236.25E-12Metabolite levelsHPOID:0001939DOID:655AintronGWASdb_trait
162907595rs656297AGrs6562975.90E-12Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162908235rs642845TCrs6428458.35E-12Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162908538rs641540AGrs6415408.35E-12Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162911341rs598253TCrs5982538.45E-12Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162911751rs11207969AGrs112079695.65E-12Metabolite levelsHPOID:0001939DOID:655AintronGWASdb_trait
162912120rs659656CGrs6596568.46E-12Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162912919rs10158897CTrs101588974.91E-12Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162912919rs10158897CTrs101588979.00E-06Lipid traitsHPOID:0003119DOID:3146|DOID:1287|DOID:9970CintronGWASdb_trait
162914978rs783291GArs7832912.97E-11Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
162915473rs11207970CTrs112079708.34E-12Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
162916796rs583609TCrs5836095.80E-12Metabolite levelsHPOID:0001939DOID:655TUTR-3GWASdb_trait
162916796rs583609TCrs5836093.23E-08Cholesterol, totalHPOID:0003107DOID:3393|DOID:3146|DOID:2349TUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000162607.12 USP1 603478