CUL5
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
11107884390rs11212484CArs112124848.20E-04Prostate cancer mortalityHPOID:0012125DOID:10283CintronGWASdb_trait
11107884390rs11212484CArs112124842.50E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
11107887274rs12277368TCrs122773686.97E-04Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287CintronGWASdb_trait
11107902017rs10890798GArs108907982.43E-05Functional impairment in major depressive disorder, bipolar disorder and schizophreniaHPOID:0007302|HPOID:0100753DOID:1470|DOID:3312|DOID:5419|DOID:5418GintronGWASdb_trait
11107904646rs10890800CTrs108908008.75E-04Rheumatoid arthritisHPOID:0001370DOID:7148CintronGWASdb_trait
11107914869rs17107685TGrs171076851.93E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
11107914869rs17107685TGrs171076852.00E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
11107924104rs17617000AGrs176170008.27E-04Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000166266.13 CUL5 601741