EPS15L1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1916471871rs8113386GCrs81133861.10E-04THYROTROPINCREATININE|CYSTATIN C|CYSTATINS|CST3 PROTEIN, HUMANKidney function and endocine traitsHPOID:0000083DOID:557GintronGWASdb_drug
1916467759rs875622AGrs8756226.77E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312TintronGWASdb_trait
1916467759rs875622AGrs8756224.00E-06White matter integrityHPOID:0002500DOID:3312|DOID:936TintronGWASdb_trait
1916471871rs8113386GCrs81133861.10E-04Kidney function and endocine traitsHPOID:0000083DOID:557GintronGWASdb_trait
1916495774rs2290669ACrs22906695.52E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312TintronGWASdb_trait
1916505106rs1870071TCrs18700719.35E-06White blood cell countHPOID:0001881DOID:74|DOID:5844GintronGWASdb_trait
1916527834rs4808047TCrs48080475.14E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312CintronGWASdb_trait
1916548375rs10411936AGrs104119363.00E-12White blood cell countHPOID:0001881DOID:74|DOID:5844AintronGWASdb_trait
1916548375rs10411936AGrs104119362.00E-07Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377AintronGWASdb_trait
1916558766rs7256818CArs72568189.96E-06White blood cell countHPOID:0001881DOID:74|DOID:5844AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000127527.13 EPS15L1 616826