Thrombophilia factors 12 mutations

The Thrombofolate Complex 12 SNP analysis is a genetic test used to study variations in genes related to folic acid metabolism and other key blood coagulation factors. The IntroLab genetics laboratory in Belgrade provides important insights into your genetic predisposition to certain diseases and health conditions through this analysis. It also offers answers regarding your response to therapy and potential preventive measures.

What are the indications?

Indications for the Thrombofolate Complex 12 SNP analysis can vary based on each patient’s specific health conditions and needs. Here are some common indications:

• History of thromboembolic diseases: If you’ve had previous cases of deep vein thrombosis (DVT), pulmonary embolism, or close relatives with similar conditions, the analysis may provide information about genetic risk factors and help assess your future risk.
• Recurrent miscarriages: If you’ve experienced multiple consecutive miscarriages, this analysis can identify genetic variations affecting blood clotting processes, helping determine the appropriate treatment or prevention approach.
• Unexplained vascular events: If you’ve had vascular events like a stroke or heart attack at a younger age, the analysis can identify genetic risk factors that may contribute to such incidents.
• Family planning: For those planning pregnancy or undergoing IVF, this analysis can offer insights into genetic factors affecting fertility, IVF success, and the risk of thrombosis during pregnancy.
• Therapeutic response: Genetic variations in the Thrombofolate Complex can influence how you respond to anticoagulant therapies such as warfarin or rivaroxaban, helping tailor the dosage and optimize treatment.

It’s important to note that these are just some potential indications, and the decision to undergo this genetic blood test should be made in consultation with a qualified healthcare professional.

Why is the Thrombofolate Complex 12 SNP analysis important?

This analysis can provide vital information about your risk for thrombosis, heart disease, miscarriages, and other conditions linked to genetic variations in the Thrombofolate Complex. Based on the results, your doctor can adjust your treatment, recommend appropriate supplements, or suggest lifestyle changes to reduce the risk of complications.

How is the Thrombofolate Complex 12 SNP analysis performed?

A small blood sample is taken from a vein for this analysis. Our expert team processes your sample and performs DNA analysis in the laboratory. Combining the latest technologies with the highest quality standards allows us to identify variations in the Thrombofolate Complex genes reliably.