F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Thrombophilia, hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5896
rs5896
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C2584620
Disease:
Thrombophilia, hereditary 		0.010 GeneticVariation BEFREE There is additive interactive effect of rs5896</span> polymorphism (CT + TT) and smoke on hereditary thrombophilia</span>. 24162564 2014