Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2153
Gene Symbol: F5
F5
0.320 GeneticVariation phenotype LHGDN Resistance to activated protein C caused by factor V Leiden mutation and orthotopic liver transplantation. 15912114 2005
Entrez Id: 2161
Gene Symbol: F12
F12
0.300 Biomarker phenotype CTD_human Defective thrombus formation in mice lacking coagulation factor XII. 16009717 2005
Entrez Id: 2621
Gene Symbol: GAS6
GAS6
0.300 Biomarker phenotype CTD_human The loss of any one of the Gas6-Rs protects mice against thromboembolism induced by collagen-epinephrine and stasis-induced thrombosis. 16564713 2006
Entrez Id: 10461
Gene Symbol: MERTK
MERTK
0.300 Therapeutic phenotype CTD_human A soluble form of the Mer receptor tyrosine kinase inhibits macrophage clearance of apoptotic cells and platelet aggregation. 17047157 2007
Entrez Id: 2
Gene Symbol: A2M
A2M
0.010 AlteredExpression phenotype LHGDN In the group of patients (IS n = 103; DVT n = 92), the risk of symptomatic thromboembolism was significantly increased with elevated alpha2MG levels, with a gradual increase per mg dL(-1). 17403113 2007
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.410 Biomarker phenotype CTD_human Essential thrombocythemia: past and present. 19636672 2009
Entrez Id: 3717
Gene Symbol: JAK2
JAK2
0.410 GeneticVariation phenotype LHGDN Recurrent refractory arterial thromboembolism associated with the Janus kinase 2 V617F mutation. 19174256 2009
Entrez Id: 2153
Gene Symbol: F5
F5
0.320 Biomarker phenotype CTD_human We investigated whether FVL was associated with TE risk in women with early-stage breast cancer who took adjuvant tamoxifen. 20554945 2010
Entrez Id: 2155
Gene Symbol: F7
F7
0.300 Biomarker phenotype CTD_human Coagulation factor VIIa (recombinant) for warfarin-induced intracranial hemorrhage. 20172985 2010
Entrez Id: 5624
Gene Symbol: PROC
PROC
0.400 GeneticVariation phenotype CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019