Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 Biomarker disease BEFREE The association between Factor V Leiden with the presence and severity of coronary artery disease. 24360889 2014
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 GeneticVariation disease BEFREE Myocardial infarction in a young patient with a previous history of repeated thrombophlebitis: combination of factor V Leiden and prothrombin G20210A gene polymorphisms with coronary artery disease. 19829138 2010
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 GeneticVariation disease BEFREE Variants of certain haemostatic genes (such as that encoding factor V Leiden) are involved in the development of venous thrombosis, but studies of such variants in coronary disease have reported apparently conflicting results. 16503463 2006
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 Biomarker disease BEFREE On the basis of these data, in women with coronary disease, the estimated number needed to screen for factor V Leiden to avoid an HRT-associated VTE during 5 years of treatment is 376. 12067913 2002
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 GeneticVariation disease BEFREE Coagulation factors II, V, VII, and X, prothrombin gene 20210G-->A transition, and factor V Leiden in coronary artery disease: high factor V clotting activity is an independent risk factor for myocardial infarction. 10195931 1999
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 GeneticVariation disease BEFREE The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease. 10070834 1999
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 Biomarker disease BEFREE The study sought to determine whether coagulation factor V Leiden (FV Leiden) plays a role in the pathogenesis of coronary artery disease and/or myocardial infarction. 9722025 1998
Entrez Id: 2153
Gene Symbol: F5
F5
0.080 GeneticVariation disease BEFREE Evidence against heterozygous coagulation factor V 1691 G-->A mutation with resistance to activated protein C being a risk factor for coronary artery disease and myocardial infarction. 8581514 1995