Normal allele: CC
Polymorphism rs2036914 is related to topics like this:
Research and publications:
19583818 Genetic variants associated with deep vein thrombosis: the F11 locus.
20174595 Personalized healthcare in clotting disorders.
21980494 Genetics of venous thrombosis: insights from a new genome wide association study.
25341889 Multilocus genetic risk scores for venous thromboembolism risk assessment.
27766050 Causes of venous thrombosis.
29995659 Venous thromboembolism risk associated with ABO, F11 and FGG loci.
32110755 Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study.
32402998 Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism.
34200207 Genetic Risk Profiling Associated with Recurrent Unprovoked Venous Thromboembolism.
34784644 The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.