Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASDB A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. 23371916 2013
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASCAT A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. 23371916 2013
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASDB Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. 23642732 2013
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASDB UGT1A1 is a major locus influencing bilirubin levels in African Americans. 22085899 2012
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASCAT Genome-wide association of serum bilirubin levels in Korean population. 20639394 2010
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASCAT Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.800 GeneticVariation GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
HIV Infections
CUI: C0019693
Disease: HIV Infections
0.700 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
0.700 GeneticVariation GWASDB Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. 23642732 2013
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
0.700 GeneticVariation GWASDB A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. 23371916 2013
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
0.700 GeneticVariation GWASDB UGT1A1 is a major locus influencing bilirubin levels in African Americans. 22085899 2012
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
0.700 GeneticVariation GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
0.700 GeneticVariation CLINVAR
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.020 GeneticVariation BEFREE The effects of gender and uridine diphosphate-glycosytransferase 1A1 (UGT1A1) genetic polymorphisms (rs4124874, rs4148323, and rs6742078) on telmisartan plasma concentration and blood pressure in Chinese patients with hypertension have been reported previously. 31254178 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.020 GeneticVariation BEFREE A genetic variant at the UGT1A1*28 locus consistently shown to be strongly associated with circulating bilirubin levels-rs6742078-was not significantly associated with blood pressure or hypertension (<i>P</i>>0.05 for all), arguing against a strong causal association of circulating bilirubin with blood pressure. 29133521 2017
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.010 GeneticVariation BEFREE The 14 single-nucleotide polymorphisms (SNPs) (<10<sup>-7</sup>) including rs6742078 of uridine diphosphoglucuronyl-transferase were selected from genome-wide association study of bilirubin level in the KCPS-II (Korean Cancer Prevention Study-II) Biobank subcohort consisting of 4793 healthy Korean and 806 stroke cases. 28389615 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE In adjusted analyses, rs6742078, which explained 19.5% of bilirubin variation, was strongly associated with total bilirubin (a 0.68-SD increase in bilirubin levels per T allele; P < 1 × 10(-122)) and was also associated with T2D risk (odds ratio [OR] 0.69 [95% CI 0.54-0.90]; P = 0.006). 25368098 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.010 GeneticVariation BEFREE UGT1A1 rs6742078 TT versus GG genotype was associated with 95% increased bilirubin levels (P < 0.001); TT versus GG genotype was associated with odds ratios (ORs) of 1.03 (95% CI, 0.96-1.11; P = 0.73) for IHD and 1.01 (95% CI, 0.92-1.12; P = 0.68) for MI. 22805420 2013
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
0.010 GeneticVariation BEFREE UGT1A1 rs6742078 TT versus GG genotype was associated with 95% increased bilirubin levels (P < 0.001); TT versus GG genotype was associated with odds ratios (ORs) of 1.03 (95% CI, 0.96-1.11; P = 0.73) for IHD and 1.01 (95% CI, 0.92-1.12; P = 0.68) for MI. 22805420 2013
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
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
0.010 GeneticVariation BEFREE UGT1A1 (rs6742078; P = .018) was associated with overall gallstone</span> risk. 20837016 2010