UBQLN1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
986289460rs7045761TCrs70457619.07E-05TOPIRAMATE|FRUCTOSEANTICONVULSANTSCognitive impairment induced by topiramateHPOID:0100543DOID:1561TintronGWASdb_drug
986324426rs12345514GTrs123455149.07E-05TOPIRAMATE|FRUCTOSEANTICONVULSANTSCognitive impairment induced by topiramateHPOID:0100543DOID:1561GnearGene-5GWASdb_drug
986289460rs7045761TCrs70457619.07E-05Cognitive impairment induced by topiramateHPOID:0100543DOID:1561TintronGWASdb_trait
986289460rs7045761TCrs70457616.73E-05Orofacial cleftsHPOID:0000202DOID:0050567TintronGWASdb_trait
986311783rs10746718AGrs107467187.49E-06HypertensionHPOID:0000822DOID:10763GintronGWASdb_trait
986324426rs12345514GTrs123455149.07E-05Cognitive impairment induced by topiramateHPOID:0100543DOID:1561GnearGene-5GWASdb_trait
986324426rs12345514GTrs123455145.77E-05Orofacial cleftsHPOID:0000202DOID:0050567GnearGene-5GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000135018.13 UBQLN1 605046