Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4552
Gene Symbol: MTRR
MTRR 		0.010 GeneticVariation phenotype LHGDN Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians. 18034637 2008
Entrez Id: 359
Gene Symbol: AQP2
AQP2 		0.010 AlteredExpression phenotype LHGDN Aquaporin 2 gene variations, risk of venous thrombosis and plasma levels of von Willebrand factor and factor VIII. 18515885 2008
Entrez Id: 7450
Gene Symbol: VWF
VWF 		0.010 AlteredExpression phenotype LHGDN Aquaporin 2 gene variations, risk of venous thrombosis and plasma levels of von Willebrand factor and factor VIII. 18515885 2008
Entrez Id: 2878
Gene Symbol: GPX3
GPX3 		0.010 GeneticVariation phenotype LHGDN Role of promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene as a risk factor for cerebral venous thrombosis. 18096833 2008
Entrez Id: 5739
Gene Symbol: PTGIR
PTGIR 		0.010 GeneticVariation phenotype LHGDN Differential association between human prostacyclin receptor polymorphisms and the development of venous thrombosis and intimal hyperplasia: a clinical biomarker study. 18551041 2008
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.010 Biomarker phenotype LHGDN Increased serum levels of leptin in retinal vein occlusion. 18679012 2008
Entrez Id: 64805
Gene Symbol: P2RY12
P2RY12 		0.010 GeneticVariation phenotype LHGDN Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism. 17707382 2008
Entrez Id: 2158
Gene Symbol: F9
F9 		0.010 Biomarker phenotype LHGDN The heparin-binding exosite of factor IXa is a critical regulator of plasma thrombin generation and venous thrombosis. 18647957 2008
Entrez Id: 183
Gene Symbol: AGT
AGT 		0.010 GeneticVariation phenotype LHGDN [Study on the association between polymorphisms in angiotensinogen gene and deep venous thrombosis]. 18543221 2008
Entrez Id: 8858
Gene Symbol: PROZ
PROZ 		0.010 GeneticVariation phenotype LHGDN The G79A polymorphism of protein Z gene is an independent risk factor for cerebral venous thrombosis. 18677630 2008
Entrez Id: 2100
Gene Symbol: ESR2
ESR2 		0.010 GeneticVariation phenotype LHGDN Association between estrogen receptor alpha and beta gene polymorphisms and deep vein thrombosis. 17184825 2007
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.010 GeneticVariation phenotype LHGDN We show that the COMT rs4680 variant modulates tHcy, and might be associated with venous thrombosis risk as well. 18064318 2007
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B 		0.010 AlteredExpression phenotype LHGDN Elevated plasma osteoprotegerin levels are associated with venous thrombosis and bleeding in patients with polycythemia vera. 15630493 2005
Entrez Id: 1636
Gene Symbol: ACE
ACE 		0.010 GeneticVariation phenotype LHGDN The angiotensin-converting-enzyme insertion/deletion polymorphism is not related to venous thrombosis. 14691571 2004
Entrez Id: 10544
Gene Symbol: PROCR
PROCR 		0.020 Biomarker phenotype LHGDN Autoantibodies against endothelial protein C receptor and the risk of a first deep vein thrombosis. 17439632 2007
Entrez Id: 2099
Gene Symbol: ESR1
ESR1 		0.020 GeneticVariation phenotype LHGDN Association between estrogen receptor alpha and beta gene polymorphisms and deep vein thrombosis. 17184825 2007
Entrez Id: 2099
Gene Symbol: ESR1
ESR1 		0.020 GeneticVariation phenotype LHGDN The ER1 haplotype does not have a strong effect on the estrogen-induced changes in haemostasis and inflammation risk markers for arterial and venous thrombosis. 16478760 2006
Entrez Id: 10544
Gene Symbol: PROCR
PROCR 		0.020 AlteredExpression phenotype LHGDN Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis. 15304035 2004
Entrez Id: 5627
Gene Symbol: PROS1
PROS1 		0.030 AlteredExpression phenotype LHGDN Only relatives with free protein S levels less than the 5th percentile (< 41 IU/dL) or less than the 2.5th percentile (< 33 IU/dL) were at higher risk of first venous thrombosis compared with the upper quartile (> 91 IU/dL); annual incidence 1.20% (95% confidence interval [CI], 0.72-1.87) and 1.81% (95% CI, 1.01-2.99), respectively; adjusted hazard ratios 5.6, (95% CI, 2.7-11.5) and 11.3 (95% CI, 5.4-23.6). 18945960 2009
Entrez Id: 7056
Gene Symbol: THBD
THBD 		0.030 Biomarker phenotype LHGDN Impaired binding of thrombin to thrombomodulin is associated with risk of deep vein thrombosis. 18590927 2008
Entrez Id: 5627
Gene Symbol: PROS1
PROS1 		0.030 GeneticVariation phenotype LHGDN A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency. 17938802 2007
Entrez Id: 7056
Gene Symbol: THBD
THBD 		0.030 GeneticVariation phenotype LHGDN Haplotype of thrombomodulin gene associated with plasma thrombomodulin level and deep vein thrombosis in the Japanese population. 16507317 2007
Entrez Id: 5627
Gene Symbol: PROS1
PROS1 		0.030 GeneticVariation phenotype LHGDN Protein S-K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients. 16461766 2006
Entrez Id: 7056
Gene Symbol: THBD
THBD 		0.030 GeneticVariation phenotype LHGDN Characterization of thrombomodulin gene mutations of the 5'-regulatory region. 12204814 2002
Entrez Id: 2161
Gene Symbol: F12
F12 		0.040 GeneticVariation phenotype LHGDN Factor XII C46T gene polymorphism and the risk of cerebral venous thrombosis. 18180442 2008