Disease: Cholelithiasis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
0.020 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
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
0.020 GeneticVariation BEFREE Second, taking advantage of mendelian randomization, we tested whether a genetic variant in the bilirubin glucoronidating enzyme UGT1A1 (rs6742078) was associated with increased plasma bilirubin levels and, in turn, with an increased risk of symptomatic gallstone disease. 23753274 2013