Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs635634
rs635634
Low density lipoprotein cholesterol measurement
T 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: rs635634
rs635634
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs635634
rs635634
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs635634
rs635634
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018

dbSNP: rs635634
rs635634
Low density lipoprotein cholesterol measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018

dbSNP: rs635634
rs635634
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs635634
rs635634
Low density lipoprotein cholesterol measurement
T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs635634
rs635634
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163

2019

dbSNP: rs635634
rs635634
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018

dbSNP: rs635634
rs635634
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018

dbSNP: rs635634
rs635634
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018

dbSNP: rs635634
rs635634
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018

dbSNP: rs635634
rs635634
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
C 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. 27989323

2017

dbSNP: rs635634
rs635634
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
T 0.700 GeneticVariation GWASCAT Genetic determinants of circulating GIP and GLP-1 concentrations. 29093273

2017

dbSNP: rs635634
rs635634
RDW - Red blood cell distribution width result
T 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414

2017

dbSNP: rs635634
rs635634
Red cell distribution width determination
T 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414

2017

dbSNP: rs635634
rs635634
Diabetes Mellitus, Non-Insulin-Dependent
T 0.700 GeneticVariation GWASCAT An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. 28566273

2017

dbSNP: rs635634
rs635634
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.700 GeneticVariation GWASCAT Genetic variation at 16q24.2 is associated with small vessel stroke. 27997041

2017

dbSNP: rs635634
rs635634
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs635634
rs635634
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs635634
rs635634
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs635634
rs635634
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs635634
rs635634
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016