SPSB4
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
3140799213rs16851055GArs168510556.00E-07Stroke (ischemic)HPOID:0002140DOID:6713GintronGWASdb_trait
3140799213rs16851055GArs168510557.00E-07Stroke (ischemic)HPOID:0002140DOID:6713GintronGWASdb_trait
3140799213rs16851055GArs168510558.00E-04Large artery strokeHPOID:0002140DOID:3393|DOID:6713GintronGWASdb_trait
3140809235rs6788334GTrs67883342.47E-04Smoking cessationHPOID:0000707DOID:0050742TintronGWASdb_trait
3140809531rs4683553TCrs46835531.73E-04Smoking cessationHPOID:0000707DOID:0050742TintronGWASdb_trait
3140810146rs6791826GArs67918263.42E-04Smoking cessationHPOID:0000707DOID:0050742AintronGWASdb_trait
3140842821rs16851066GArs168510665.37E-06OsteoarthritisHPOID:0002758DOID:8398GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000175093.4 SPSB4 611660