UBASH3A
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2143822402rs11909987CArs119099873.62E-05ACETAMINOPHEN|GLUTATHIONEN-ACETYL-4-BENZOQUINONEIMINE|RNA, MESSENGER|IMINES|BENZOQUINONESResponse to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409A,CnearGene-5GWASdb_drug
2143823736rs9784215CArs97842152.73E-05ACETAMINOPHEN|GLUTATHIONEN-ACETYL-4-BENZOQUINONEIMINE|RNA, MESSENGER|IMINES|BENZOQUINONESResponse to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409CnearGene-5GWASdb_drug
2143826344rs3746923CTrs37469232.56E-05ACETAMINOPHEN|GLUTATHIONEN-ACETYL-4-BENZOQUINONEIMINE|RNA, MESSENGER|IMINES|BENZOQUINONESResponse to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409TintronGWASdb_drug
2143822402rs11909987CArs119099873.62E-05Response to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409A,CnearGene-5GWASdb_trait
2143823736rs9784215CArs97842152.73E-05Response to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409CnearGene-5GWASdb_trait
2143825519rs7283281GCrs72832818.80E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
2143826344rs3746923CTrs37469232.56E-05Response to acetaminophen (hepatotoxicity)HPOID:0001392DOID:409TintronGWASdb_trait
2143836186rs11203203GArs112032032.37E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
2143836186rs11203203GArs112032032.00E-09Type 1 diabetesHPOID:0100651DOID:9744AintronGWASdb_trait
2143836186rs11203203GArs112032031.00E-09VitiligoHPOID:0001045DOID:12306AintronGWASdb_trait
2143836186rs11203203GArs112032034.00E-06Rheumatoid arthritisHPOID:0001370DOID:7148AintronGWASdb_trait
2143836186rs11203203GArs112032031.00E-08Celiac disease and Rheumatoid arthritisHPOID:0001438|HPOID:0001370DOID:10608|DOID:7148AintronGWASdb_trait
2143836186rs11203203GArs112032031.44E-07Type 1 diabetesHPOID:0100651DOID:9744AintronGWASdb_trait
2143836186rs11203203GArs112032030.000029Primary sclerosing cholangitisHPOID:0001080DOID:14268AintronGWASdb_trait
2143836186rs11203203GArs112032035.81E-12VitiligoHPOID:0001045DOID:12306AintronGWASdb_trait
2143836186rs11203203GArs112032038.54E-08Primary sclerosing cholangitisHPOID:0001080DOID:14268AintronGWASdb_trait
2143836390rs9976767AGrs99767672.00E-08Type 1 diabetesHPOID:0100651DOID:9744GintronGWASdb_trait
2143836390rs9976767AGrs99767672.00E-08Multiple 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
2143836390rs9976767AGrs99767670.0004Primary sclerosing cholangitisHPOID:0001080DOID:14268GintronGWASdb_trait
2143841328rs3788013CArs37880131.00E-07Type 1 diabetes autoantibodiesHPOID:0100651DOID:9744A,CintronGWASdb_trait
2143848521rs2839511GArs28395112.48E-05VitiligoHPOID:0001045DOID:12306GintronGWASdb_trait
2143848521rs2839511GArs28395111.17E-08VitiligoHPOID:0001045DOID:12306GintronGWASdb_trait
2143853789rs883390AGrs8833901.90E-06Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
2143855067rs1893592ACrs18935923.00E-09Celiac diseaseHPOID:0001438DOID:10608AintronGWASdb_trait
2143855067rs1893592ACrs18935921.30E-04Rheumatoid arthritisHPOID:0001370DOID:7148AintronGWASdb_trait
2143855067rs1893592ACrs18935927.00E-12Rheumatoid arthritisHPOID:0001370DOID:7148AintronGWASdb_trait
2143855067rs1893592ACrs18935929.80E-09Rheumatoid arthritisHPOID:0001370DOID:7148AintronGWASdb_trait
2143865297rs2839517CTrs28395175.92E-05Myopia (pathological)HPOID:0000545DOID:11830CintronGWASdb_trait
2143865313rs2839518TCrs28395189.30E-05Eosinophil countsHPOID:0001879|HPOID:0001658|HPOID:0002099DOID:999|DOID:2841|DOID:5844TintronGWASdb_trait
2143867787rs3827233GCrs38272331.10E-05Urinary metabolitesHPOID:0000079DOID:557GUTR-3GWASdb_trait
2143867844rs2839519GArs28395190.00000019Confectionary intakeHPOID:0001513DOID:9970GnearGene-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000160185.14 UBASH3A 605736