rs552953108, F2

N. diseases: 16
Disease: Sinus Thrombosis, Intracranial ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sinus Thrombosis, Intracranial
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
0.010 GeneticVariation BEFREE Over a 3 year period the R506Q mutation in the factor V (FV) FV:Q506 gene, FV, factor XII (FXII), prothrombin, protein C, protein S, antithrombin, heparin cofactor II, anticardiolipin antibodies and lipoprotein (a) (Lp(a)) were measured in 32 infants and children with sinus thrombosis. 9686815 1998