Sep 28, 2021 · It is a genetic mutation in your Factor II gene that makes it create too much prothrombin (coagulation factor II), and you end up with a higher risk of developing blood clots …

It is due to a specific gene mutation in which a guanine is changed to an adenine at position 20210 of the DNA of the prothrombin gene. Other blood clotting pathway mutations that …

All individuals make the prothrombin (also called factor two) protein that helps blood clot. However, there are certain individuals who have a DNA mutation in the gene used to make …

INTRODUCTION Prothrombin G20210A is the second most common inherited thrombophilia after factor V Leiden. Challenging clinical issues include the decisions regarding when to test for …

A single nucleotide mutation in one (or, less commonly, both) of the prothrombin genes at position 20210 results in increased plasma prothrombin levels (with potentially increased thrombin …

Sep 6, 2024 · Learn about the role of the prothrombin gene and how a mutation in this gene can increase your risk of thrombosis and other complications.

Several variants (also called mutations) in the F2 gene have been found to cause prothrombin deficiency, a bleeding disorder that slows the clotting process. Most of these variants change …

The factor II c.*97G>A (prothrombin G20210A) gene variant is the second most common genetic defect influencing the risk of venous thromboembolism (VTE), with factor V Leiden being the …

for the prothrombin 20210 mutation, also called factor II mutation, may have been offered by your doctor because you or someone in your family, has had (1) a blood clot in one of the deep …

Jan 19, 2024 · The Prothrombin 20210 mutation, also known as the Factor II mutation, is a genetic alteration that increases the risk of developing blood clots. This mutation leads to …