Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. 31393916 2019
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. 30670697 2019
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809 2016
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943 2015
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125 2013
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. 23726366 2013
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study. 23100282 2013
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. 22629316 2012
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.100 GeneticVariation phenotype GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009