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Lithium

Prothrombin (Factor II) Gene Mutation - G20210A

The Prothrombin (Factor II) Gene Mutation - G20210A test is a genetic test that is used to identify a specific mutation (G20210A) in the prothrombin gene, also known as Factor II. Prothrombin is a protein that plays a crucial role in the blood clotting process, helping to prevent excessive bleeding.

The G20210A mutation in the prothrombin gene is associated with an increased production of prothrombin, leading to a heightened risk of forming abnormal blood clots. These clots can obstruct blood vessels, leading to conditions like deep vein thrombosis or pulmonary embolism. Identifying this mutation can be important for people with a personal or family history of abnormal blood clotting, as it can help guide treatment and prevention strategies.

  • Test NameProthrombin (Factor II) Gene Mutation - G20210A
  • Sample TypeBlood
  • Preparations RequiredNo special preparation is needed for this test. Continue your usual diet and medications unless directed otherwise by your healthcare provider.
  • Report Time3 days
Why might my doctor order a Prothrombin (Factor II) Gene Mutation - G20210A test?

Your doctor may order this test if you have a history of abnormal blood clotting, or if you have a family history of the condition. It's also commonly ordered if you're planning to start a course of medication that can increase the risk of blood clots.

What does a positive result mean?

A positive result indicates the presence of the G20210A mutation in the prothrombin gene. This means you may have an increased risk of developing abnormal blood clots.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

This test doesn't diagnose a disease, but it identifies a genetic risk factor for abnormal blood clotting, which could lead to conditions like deep vein thrombosis or pulmonary embolism.

The test involves drawing a small amount of blood from your arm. This is a routine procedure and typically causes minimal discomfort.

The test is generally safe with minimal risks, which may include slight pain or bruising at the injection site. Serious complications are rare.

No special preparations are needed. You should continue your normal diet and take your medications as usual unless instructed otherwise by your healthcare provider.

The results of this test are generally accurate and reliable. However, certain laboratory errors can potentially affect the results.

If you test positive for the G20210A mutation, your doctor will likely recommend steps to manage your increased risk of blood clotting. This could include lifestyle changes or medication.

Yes, the test can be performed during pregnancy. In fact, it may be particularly useful if you're pregnant, as the risk of blood clots can increase during pregnancy.

Yes, if you carry the G20210A mutation, there is a chance your children might inherit it. Genetic counseling can provide more detailed information

This test is highly reliable in detecting the presence of the G20210A mutation in the prothrombin gene.

Coverage can vary greatly, so it's important to check with your insurance company.

No, the test requires a blood sample to be drawn, which must be done in a clinical setting.

Anyone with a personal or family history of abnormal blood clotting should consider this test, especially before starting certain medications or planning a pregnancy.

No, the results of this test are genetic, so they can't be influenced by lifestyle or diet. Understanding the presence of the G20210A mutation can be essential in predicting and managing the risk of abnormal blood clotting. It's always important to discuss the results of this test with your healthcare provider to understand what they mean for your specific situation.

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