Molecular Pathology Laboratory Network

MPLN offers specialized genetic tests to distinguish heterogeneous causes of thrombosis in patients presenting with early onset, familial, recurrent or unprovoked venous thrombotic events.

The ThromboFLEX™ Profile simultaneously analyzes Factor V, Factor II and MTHFR genes for the common mutations / polymorphisms reported to be associated with an increased risk for venous and/or arterial thromboses.

Test Information and Specimen Requirements

• Factor II (Prothrombin) G20210A mutation »
• Factor V (Leiden) G1691A/R506Q mutation »
• Methylenetetrahydrofolate reductase mutation (MTHFR) C667T and A1298C mutations »

For more information about ThromboFLEX, contact a client service specialist at 800.932.2943.

Our Testing Resources

ThromboFLEX™ Profile information