UBLCP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5158690951rs4921437TCrs49214371.42E-04Lung function (forced expiratory volume in 1 second)HPOID:0002088DOID:850TintronGWASdb_trait
5158691793rs10515780CGrs105157807.13E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
5158697131rs2420825CTrs24208252.98E-04Lung function (forced expiratory flow between 25% and 75% of forced vital capacity)HPOID:0002088DOID:850T,CintronGWASdb_trait
5158697131rs2420825CTrs24208253.24E-04Lung function (forced expiratory volume in 1 second)HPOID:0002088DOID:850T,CintronGWASdb_trait
5158706713rs13153734CTrs131537348.10E-07Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
5158708065rs6887080AGrs68870809.41E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
5158709277rs10515782CTrs105157825.79E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
5158709277rs10515782CTrs105157821.47E-04Statin-induced myopathyHPOID:0001637DOID:0080000TintronGWASdb_trait
5158710768rs10042630ATrs100426305.23E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
5158711219rs4921209AGrs49212098.30E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000164332.7 UBLCP1 609867