Risk of thrombosis (baseline, abbreviated) (F II, F V, MTHFR, PAI-I (SERPINE1) (4)

Genes’ polymorphisms (changes) of the coagulation system are the most common reason of thrombosis development in women. Outcomes of this study will help to assess the genetic risk of thrombosis might  be exacerbated by the concomitant clinical and environmental factors presence.

The constancy of genetic pattern enables to use this information in line to arrange preventive measures aimed to adjust the blood coagulation system in order to reduce the risk of thrombosis.