Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4420638
rs4420638
A 0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973

2019

dbSNP: rs4420638
rs4420638
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs4420638
rs4420638
A 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018

dbSNP: rs4420638
rs4420638
A 0.800 GeneticVariation GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809

2016

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT THOC5: a novel gene involved in HDL-cholesterol metabolism. 24023261

2013

dbSNP: rs4420638
rs4420638
0.800 GeneticVariation GWASDB Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study. 23100282

2013

dbSNP: rs4420638
rs4420638
0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 18193043

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB LDL-cholesterol concentrations: a genome-wide association study. 18262040

2008

dbSNP: rs4420638
rs4420638
0.800 GeneticVariation GWASDB Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. 18802019

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASDB Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. 18193044

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. 18193044

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT LDL-cholesterol concentrations: a genome-wide association study. 18262040

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 18193043

2008

dbSNP: rs4420638
rs4420638
0.800 GeneticVariation GWASCAT Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. 18802019

2008

dbSNP: rs4420638
rs4420638
G 0.800 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007