F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Coronary heart disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0010068
Disease:
Coronary heart disease 		0.040 GeneticVariation BEFREE VTE and CHD incidence were compared with adjustment for cardiovascular risk factors and prothrombotic gene polymorphisms of coagulation factors II/prothrombin (G20210A) and V (G1691A). 20737565 2010
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0010068
Disease:
Coronary heart disease 		0.040 GeneticVariation BEFREE Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran. 19349859 2009
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0010068
Disease:
Coronary heart disease 		0.040 GeneticVariation BEFREE Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease. 15353918 2004
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0010068
Disease:
Coronary heart disease 		0.040 GeneticVariation BEFREE To investigate the prevalence of the G20210A prothrombin and G1691A factor V gene variants in patients with acute coronary syndrome stratified according to risk factor profile and to extent of coronary disease, in comparison with matched healthy controls. 11741359 2002