WDR7
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1854319099rs477415ATrs4774156.26E-04Coronary heart diseaseHPOID:0001677DOID:3393TintronGWASdb_trait
1854341968rs633235GArs6332354.90E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
1854365965rs12953387CTrs129533871.91E-04Coronary heart diseaseHPOID:0001677DOID:3393CintronGWASdb_trait
1854385713rs11664579AGrs116645794.84E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
1854388902rs2080681TGrs20806812.43E-04Coronary heart diseaseHPOID:0001677DOID:3393AintronGWASdb_trait
1854397622rs17750015TCrs177500158.00E-06Depression and alcohol dependenceHPOID:0000716DOID:303|DOID:1596TintronGWASdb_trait
1854480479rs9946253ACrs99462534.74E-04Parkinson's diseaseHPOID:0001300DOID:14330CintronGWASdb_trait
1854555423rs1542006CGrs15420063.73E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
1854557209rs6566839CGrs65668391.45E-04Rheumatoid Arthritis (Cyclic citrullinated peptide positive)HPOID:0001370DOID:7148CintronGWASdb_trait
1854567759rs2083020AGrs20830201.40E-04Rheumatoid Arthritis (Cyclic citrullinated peptide positive)HPOID:0001370DOID:7148AintronGWASdb_trait
1854581904rs2043686AGrs20436863.32E-05Rheumatoid Arthritis (Cyclic citrullinated peptide positive)HPOID:0001370DOID:7148TintronGWASdb_trait
1854591871rs8094838AGrs80948387.32E-04Alzheimer's diseaseHPOID:0002511DOID:10652AintronGWASdb_trait
1854649711rs1657415GArs16574158.66E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
1854658824rs1657421CTrs16574211.71E-05HemoglobinHPOID:0011902DOID:2860CintronGWASdb_trait
1854658824rs1657421CTrs16574217.99E-05HematocritHPOID:0000822DOID:10763CintronGWASdb_trait
1854659855rs1787463AGrs17874638.19E-05HemoglobinHPOID:0011902DOID:2860AintronGWASdb_trait
1854663205rs1787479CGrs17874796.52E-04Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
1854675357rs17830589GTrs178305894.73E-05Serum albumin levelHPOID:0010876DOID:557|DOID:409|DOID:1287GintronGWASdb_trait
1854687813rs2278495GArs22784957.94E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
1854690271rs722091GArs7220912.62E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
1854690287rs722090CTrs7220902.40E-04Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
1854696407rs1657396TCrs16573969.54E-04Multiple complex diseasesHPOID:0000118NAGUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000091157.13 WDR7 613473