USP2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
11119235404rs2195525CTrs21955252.00E-06URIC ACIDGLUCOSE|INHIBINSUrate levelsHPOID:0000079DOID:13189CintronGWASdb_drug
11119235404rs2195525CTrs21955252.00E-06Urate levelsHPOID:0000079DOID:13189CintronGWASdb_trait
11119241120rs514808AGrs5148085.28E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312CintronGWASdb_trait
11119246896rs576945GArs5769458.83E-06Blood PressureHPOID:0011025DOID:10763CintronGWASdb_trait
11119246896rs576945GArs5769459.44E-05Blood PressureHPOID:0011025DOID:10763CintronGWASdb_trait
11119252151rs565296CTrs5652961.02E-05Blood PressureHPOID:0011025DOID:10763GintronGWASdb_trait
11119252151rs565296CTrs5652966.70E-05Blood PressureHPOID:0011025DOID:10763GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000036672.15 USP2 604725