Factor V Mutation Screening (F5 - G1691A) Test
Short Name: Factor V Mutation Screening
Also known as: F5 G1691A Mutation Test, Factor V Leiden Mutation Screening
Factor V Mutation Screening (F5 - G1691A) Test test available at DNA Labs India for ₹6,000. Uses Real Time PCR on Peripheral blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of Factor V Mutation Screening is to detect the G1691A mutation in the Factor V gene, which is associated with an increased risk of venous thromboembolism. This test helps in diagnosing hereditary thrombophilia, guiding treatment decisions, and implementing preventive measures for at-risk individuals.
- Test Code
- 3000
- Price
- ₹6,000
- Sample Type
- Peripheral blood
- Result Time
- 3-4 days
- Fasting Required
- No
- Method
- Real Time PCR
Sample Collection
No specific preparation is required. Bring a doctor's prescription if applicable, and inform the healthcare provider about any medications or recent medical procedures.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in your arm using a needle. The process is quick and typically takes a few minutes.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. You may resume normal activities immediately.
Timeline: 3-4 days
Patient Instructions
About This Test
Who Should Get This Test
The purpose of Factor V Mutation Screening is to detect the G1691A mutation in the Factor V gene, which is associated with an increased risk of venous thromboembolism. This test helps in diagnosing hereditary thrombophilia, guiding treatment decisions, and implementing preventive measures for at-risk individuals.
How to Prepare
- No fasting required for this test
- Bring a valid doctor's prescription if available, though it may not be required for certain cases like surgery or pregnancy planning
- Inform the phlebotomist about any recent blood transfusions or medications
- Stay hydrated and wear loose clothing for easy access to the arm
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for individuals with a family history of blood clots or unexplained thrombotic events, aiding in early intervention and risk management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood sample
- Incorrect sample type or container
- Insufficient sample volume
- Labeled incorrectly or missing patient information
Understanding Your Results
Mutation Detected
Indicates an increased risk of developing blood clots. Consult a doctor for further evaluation, lifestyle advice, and possible anticoagulant therapy.
No Mutation Detected
Suggests a lower genetic risk for Factor V Leiden-related thrombophilia, but other risk factors may still be present. Discuss with a healthcare provider for comprehensive assessment.
Consult a doctor if you have symptoms of blood clots (e.g., pain, swelling, chest pain), a family history of thrombophilia, or if you are planning surgery or pregnancy. Also, seek medical advice after receiving test results for personalized management.
Limitations
- ⚠This test only screens for the G1691A mutation and may not detect other rare Factor V mutations
- ⚠Does not assess other genetic or acquired causes of thrombophilia
- ⚠Results should be interpreted in conjunction with clinical history and other tests
Risks & Considerations
- ●Minor bruising or pain at the puncture site
- ●Rare risk of infection or excessive bleeding
- ●Fainting or dizziness in some individuals
Interfering Factors
- ●Recent blood transfusions or bone marrow transplants may interfere with test results
- ●Contamination of the sample
- ●Certain medications affecting DNA integrity
Compare With Similar Tests
| Test | Factor V Mutation Screening (F5 - G1691A) | Prothrombin Gene Mutation Test | Antithrombin III Activity Test | Protein C and S Assay |
|---|---|---|---|---|
| Comparison | Factor V Mutation Screening (F5 - G1691A) | Screens for the G20210A mutation in the prothrombin gene, another common cause of thrombophilia. | Measures antithrombin III levels, which if low, can increase clotting risk. | Evaluates protein C and S deficiencies, which are natural anticoagulants. |
Frequently Asked Questions
What is Factor V Mutation Screening?
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