Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs579459
rs579459
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013

dbSNP: rs579459
rs579459
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013

dbSNP: rs579459
rs579459
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568

2012

dbSNP: rs579459
rs579459
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
T 0.800 GeneticVariation GWASDB Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. 22001757

2011

dbSNP: rs579459
rs579459
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
C 0.800 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011

dbSNP: rs579459
rs579459
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs579459
rs579459
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement
C 0.800 GeneticVariation GWASDB Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. 19729612

2009

dbSNP: rs579459
rs579459
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
C 0.700 GeneticVariation GWASDB Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014

dbSNP: rs579459
rs579459
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943

2013

dbSNP: rs579459
rs579459
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASDB Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. 23300278

2013

dbSNP: rs579459
rs579459
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013

dbSNP: rs579459
rs579459
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178

2013

dbSNP: rs579459
rs579459
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013

dbSNP: rs579459
rs579459
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 GeneticVariation GWASDB A genome-wide association study of circulating galectin-3. 23056639

2012

dbSNP: rs579459
rs579459
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
0.700 GeneticVariation GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575

2012

dbSNP: rs579459
rs579459
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 GeneticVariation GWASDB A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. 22291609

2012

dbSNP: rs579459
rs579459
Corpuscular Hemoglobin Concentration Mean
T 0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012

dbSNP: rs579459
rs579459
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661

2012