UBXN7
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
3196088464rs6764533GArs67645330.0002Diabetic retinopathy in Type 2 diabetes mellitus, ETDRS grade>=30HPOID:0000819|HPOID:0000488|HPOID:0005978DOID:8947|DOID:9352GintronGWASdb_trait
3196095560rs11920918GArs119209184.26E-10Cholesterol, totalHPOID:0003107DOID:3393|DOID:3146|DOID:2349GintronGWASdb_trait
3196095560rs11920918GArs119209188.70E-23LDL cholesterolHPOID:0010979DOID:1936|DOID:3393GintronGWASdb_trait
3196118621rs6583305ATrs65833050.0002Diabetic retinopathy in Type 2 diabetes mellitus, ETDRS grade>=30HPOID:0000819|HPOID:0000488|HPOID:0005978DOID:8947|DOID:9352TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000163960.11 UBXN7 616379