Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9411377
rs9411377
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. 31676865

2019

dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
T 0.820 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019

dbSNP: rs687289
rs687289
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
A 0.800 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019

dbSNP: rs8176749
rs8176749
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
T 0.700 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019

dbSNP: rs507666
rs507666
ABO
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639

2019

dbSNP: rs505922
rs505922
ABO
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
C 0.700 GeneticVariation GWASCAT Genome-wide association study of peripheral artery disease in the Million Veteran Program. 31285632

2019

dbSNP: rs507666
rs507666
ABO
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: rs550057
rs550057
ABO
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs550057
rs550057
ABO
Low density lipoprotein cholesterol measurement
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs507666
rs507666
ABO
Low density lipoprotein cholesterol measurement
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019

dbSNP: rs2519093
rs2519093
ABO
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement
T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. 31217265

2019

dbSNP: rs492488
rs492488
ABO
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
G 0.700 GeneticVariation GWASCAT Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. 31070104

2019

dbSNP: rs550057
rs550057
ABO
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
C 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462

2019

dbSNP: rs676996
rs676996
ABO
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
T 0.700 GeneticVariation GWASCAT Assessing the causal association of glycine with risk of cardio-metabolic diseases. 30837465

2019

dbSNP: rs507666
rs507666
ABO
Low density lipoprotein cholesterol measurement
A 0.700 GeneticVariation GWASCAT Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. 30670697

2019

dbSNP: rs8176746
rs8176746
ABO
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs8176746
rs8176746
ABO
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs550057
rs550057
ABO
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs550057
rs550057
ABO
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs2519093
rs2519093
ABO
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs2519093
rs2519093
ABO
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs187099314
rs187099314
ABO
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs687289
rs687289
ABO
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
A 0.800 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737

2019

dbSNP: rs8176719
rs8176719
ABO
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737

2019

dbSNP: rs8176719
rs8176719
ABO
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement
0.700 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737

2019