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Factor II prothrombin mutation

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Factor II prothrombin mutation

Accredited Facility E-report Qualified Specialists

This test is done to identify a mutation in the prothrombin (Factor II) gene that can increase the risk of abnormal blood clot formation. It helps assess inherited risk for conditions such as deep vein thrombosis or pulmonary embolism, especially in individuals with a personal or family history of clotting disorders.

  • If you have a history of unexplained blood clots.
  • If there is a family history of clotting disorders.
  • If you have experienced clotting at a young age or without clear cause.
  • If a healthcare provider recommends thrombophilia screening.
  • No fasting is required.
  • No special preparation is usually needed.
  • Genetic counseling may be recommended before or after testing.
  • Follow any instructions provided by the laboratory or healthcare provider.
    • Factor II prothrombin mutation
    No labs currently offering this test.