PDZRN4
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1241721430rs1880887CTrs18808878.69E-05TOPIRAMATE|FRUCTOSEANTICONVULSANTSCognitive impairment induced by topiramateHPOID:0100543DOID:1561GintronGWASdb_drug
1241723120rs11180828AGrs111808284.42E-05TAMSULOSINADRENERGIC ALPHA-1 RECEPTOR ANTAGONISTS|SULFONAMIDESSerum tamsulosin hydrochloride concentrationHPOID:0012220DOID:11132GintronGWASdb_drug
1241602355rs2043134AGrs20431340.000118Breast cancer early age of onsetHPOID:0003002DOID:1612GintronGWASdb_trait
1241614599rs12367762GTrs123677624.00E-06Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
1241614599rs12367762GTrs123677628.94E-05Bipolar disorderHPOID:0007302DOID:3312GintronGWASdb_trait
1241614599rs12367762GTrs123677626.38E-05Response to taxane treatment (placlitaxel)HPOID:0100526DOID:1324GintronGWASdb_trait
1241721235rs1880889ACrs18808891.96E-08Alkaline phosphatase (ALP)HPOID:0001392DOID:409GintronGWASdb_trait
1241721430rs1880887CTrs18808871.00E-10Protein quantitative trait lociHPOID:0000118NAGintronGWASdb_trait
1241721430rs1880887CTrs18808878.69E-05Cognitive impairment induced by topiramateHPOID:0100543DOID:1561GintronGWASdb_trait
1241723120rs11180828AGrs111808287.88E-05Panic disorderHPOID:0100851DOID:594GintronGWASdb_trait
1241723120rs11180828AGrs111808282.50E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
1241723120rs11180828AGrs111808280.0000442Panic disorderHPOID:0100851DOID:594GintronGWASdb_trait
1241723120rs11180828AGrs111808284.42E-05Serum tamsulosin hydrochloride concentrationHPOID:0012220DOID:11132GintronGWASdb_trait
1241726649rs1405553TCrs14055535.09E-04Myopia (pathological)HPOID:0000545DOID:11830GintronGWASdb_trait
1241727678rs1000147ACrs10001478.26E-06Bone mineral densityHPOID:0004348DOID:0080011GintronGWASdb_trait
1241747428rs10785246CTrs107852464.67E-05Alcohol and nictotine co-dependenceHPOID:0000707DOID:0050741|DOID:0050742TintronGWASdb_trait
1241755479rs10506189TCrs105061891.59E-05Bone mineral densityHPOID:0004348DOID:0080011CintronGWASdb_trait
1241760767rs10880063TCrs108800635.41E-05Lung function (forced vital capacity)HPOID:0002088DOID:850TintronGWASdb_trait
1241766492rs11180863GTrs111808635.62E-05Lung function (forced vital capacity)HPOID:0002088DOID:850GintronGWASdb_trait
1241768111rs10880067GArs108800675.41E-05Lung function (forced vital capacity)HPOID:0002088DOID:850GintronGWASdb_trait
1241797386rs12305552GArs123055522.01E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
1241816002rs987823TCrs9878235.20E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
1241819215rs1350430TCrs13504303.96E-04Myopia (pathological)HPOID:0000545DOID:11830TintronGWASdb_trait
1241822199rs1458165GArs14581652.38E-04Myopia (pathological)HPOID:0000545DOID:11830GintronGWASdb_trait
1241833162rs2730828AGrs27308283.96E-04Myopia (pathological)HPOID:0000545DOID:11830TintronGWASdb_trait
1241848356rs1870286CArs18702866.09E-04Myopia (pathological)HPOID:0000545DOID:11830AintronGWASdb_trait
1241893994rs17129414AGrs171294141.57E-06Asthma (childhood onset)HPOID:0002099DOID:2841AintronGWASdb_trait
1241903274rs12423463GArs124234635.38E-04StrokeHPOID:0001297DOID:6713GintronGWASdb_trait
1241932438rs725527CTrs7255278.78E-05Cognitive performanceHPOID:0100543DOID:1561CintronGWASdb_trait
1241935609rs11180989CArs111809899.95E-05Cognitive performanceHPOID:0100543DOID:1561CintronGWASdb_trait
1241952824rs157972GArs1579727.42E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
1241952824rs157972GArs1579728.27E-05Femoral neck bone geometryHPOID:0003367DOID:0080011AintronGWASdb_trait
1241965861rs1458175ACrs14581752.00E-06Multiple 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:2377GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000165966.14 PDZRN4 609730