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 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
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