Disease: Gilbert Disease (disorder) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
0.010 GeneticVariation BEFREE The UGT1A1 Gilbert syndrome variant rs6742078 is associated with gallstone disease in men; further studies are required regarding the sex-specific physiology of bilirubin and bile acid metabolism. 20837016 2010