Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1 		0.340 GeneticVariation phenotype LHGDN Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis. 17244682 2007
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1 		0.340 GeneticVariation phenotype LHGDN Five novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis. 12894857 2003
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1 		0.340 GeneticVariation phenotype LHGDN Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiency. 11686319 2001
Entrez Id: 2157
Gene Symbol: F8
F8 		0.330 GeneticVariation phenotype LHGDN Absence of mutations at the APC interacting sites of factor VIII in Caucasians. 11848448 2002
Entrez Id: 2157
Gene Symbol: F8
F8 		0.330 GeneticVariation phenotype LHGDN The protective effect of the factor XIII Val34Leu mutation on the risk of deep venous thrombosis is dependent on the fibrinogen level. 15869621 2005
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.330 GeneticVariation phenotype LHGDN Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians. 17287626 2007
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.330 GeneticVariation phenotype LHGDN Methylenetetrahydrofolate reductase (MTHFR-677 and MTHFR-1298) genotypes and haplotypes and plasma homocysteine levels in patients with occlusive artery disease and deep venous thrombosis. 18800176 2008
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.330 GeneticVariation phenotype LHGDN Mesenteric venous thrombosis with bowel infarction and hyperhomocysteinemia due to homozygous methylenetetrahydrofolate reductase C677T genotype. 19000982 2009
Entrez Id: 2162
Gene Symbol: F13A1
F13A1 		0.320 GeneticVariation phenotype LHGDN The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients. 17195962 2008
Entrez Id: 7035
Gene Symbol: TFPI
TFPI 		0.320 GeneticVariation phenotype LHGDN These results indicate that the TFPI -33T->C and -399C->T polymorphisms are significantly associated with venous thrombosis in the presence of other risk factors, especially APS, and may be clinically relevant in patients who are prone to hypercoagulability. 17762532 2007
Entrez Id: 2162
Gene Symbol: F13A1
F13A1 		0.320 GeneticVariation phenotype LHGDN The V34L polymorphism of factor XIII and peripheral arterial disease. 11941274 2002
Entrez Id: 7035
Gene Symbol: TFPI
TFPI 		0.320 GeneticVariation phenotype LHGDN Analysis of a T-287C polymorphism in the tissue factor pathway inhibitor gene and identification of a repressor element in the promoter. 17931693 2008
Entrez Id: 51156
Gene Symbol: SERPINA10
SERPINA10 		0.310 GeneticVariation phenotype LHGDN A nonsense polymorphism in the protein Z-dependent protease inhibitor increases the risk for venous thrombosis. 16527896 2006
Entrez Id: 2243
Gene Symbol: FGA
FGA 		0.300 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1 		0.220 GeneticVariation phenotype LHGDN Association of 4G/5G polymorphism in PAI1 promoter with PAI1 level in deep vein thrombosis. 16331557 2005
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1 		0.220 GeneticVariation phenotype LHGDN Association between the plasminogen activator inhibitor-1 4G/5G polymorphism and venous thrombosis. A meta-analysis. 17549286 2007
Entrez Id: 3586
Gene Symbol: IL10
IL10 		0.110 GeneticVariation phenotype LHGDN Multivariate logistic regression analysis showed that IL-10 G13 and G10 alleles are independent risk factors for venous thrombosis (Odds ratio:OR = 3.33, p = 0.003 and OR = 2.83, p = 0.03, respectively). 16807647 2006
Entrez Id: 285440
Gene Symbol: CYP4V2
CYP4V2 		0.110 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 2266
Gene Symbol: FGG
FGG 		0.110 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 2266
Gene Symbol: FGG
FGG 		0.110 GeneticVariation phenotype LHGDN Polymorphism 10034C>T is located in a region regulating polyadenylation of FGG transcripts and influences the fibrinogen gamma'/gammaA mRNA ratio. 17403086 2007
Entrez Id: 23360
Gene Symbol: FNBP4
FNBP4 		0.100 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 5795
Gene Symbol: PTPRJ
PTPRJ 		0.100 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 29922
Gene Symbol: NME7
NME7 		0.100 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 10658
Gene Symbol: CELF1
CELF1 		0.100 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
Entrez Id: 169436
Gene Symbol: STKLD1
STKLD1 		0.100 GeneticVariation phenotype GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012