Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT Genome-wide analysis of genetic predisposition to Alzheimer's disease and related sex disparities. 30636644

2019

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
A 0.820 GeneticVariation GWASCAT Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. 26830138

2016

dbSNP: rs4420638
rs4420638
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT Genome-wide association analysis of age-at-onset in Alzheimer's disease. 22005931

2012

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT Genome-wide association study of Alzheimer's disease. 22832961

2012

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. 17998437

2008

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT Sorl1 as an Alzheimer's disease predisposition gene? 17975299

2008

dbSNP: rs4420638
rs4420638
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.820 GeneticVariation GWASCAT A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. 17474819

2007

dbSNP: rs4420638
rs4420638
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
A 0.810 GeneticVariation GWASCAT Seven new loci associated with age-related macular degeneration. 23455636

2013

dbSNP: rs4420638
rs4420638
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs4420638
rs4420638
Low density lipoprotein cholesterol measurement
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
High density lipoprotein measurement
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
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

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

2018

dbSNP: rs4420638
rs4420638
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
A 0.800 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399

2018

dbSNP: rs4420638
rs4420638
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
A 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018

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

2018

dbSNP: rs4420638
rs4420638
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
A 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018

dbSNP: rs4420638
rs4420638
High density lipoprotein measurement
A 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899

2017

dbSNP: rs4420638
rs4420638
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
A 0.800 GeneticVariation GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809

2016

dbSNP: rs4420638
rs4420638
High density lipoprotein measurement
0.800 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

dbSNP: rs4420638
rs4420638
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

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

2016

dbSNP: rs4420638
rs4420638
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
A 0.800 GeneticVariation GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809

2016

dbSNP: rs4420638
rs4420638
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016