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DNA Labs India

Factor V Mutation Screening (F5 - G1691A) Test

DNA Labs India | ISO 9001:2015 Certified

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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

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
Step 1

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

Step 2

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.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. You may resume normal activities immediately.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:No special preparation needed. Ensure you have a doctor's prescription if required for insurance or specific cases.
2
During the Test:A small blood sample is collected from your arm. The procedure is minimally invasive and quick.
3
After the Test:You can resume normal activities immediately. Apply a bandage to the puncture site if needed.

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 — 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 TypePeripheral blood
Sample Volume2ml
ContainerEDTA Vacutainer
Collection MethodVenipuncture

Sample Stability

Stable at room temperature for up to 24 hours
Refrigerate at 2-8°C if analysis is delayed beyond 24 hours
Avoid repeated freeze-thaw cycles
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Incorrect sample type or container
  • Insufficient sample volume
  • Labeled incorrectly or missing patient information

Understanding Your Results

Results from Factor V Mutation Screening indicate the presence or absence of the G1691A mutation. Interpretation should be done by a qualified healthcare professional in the context of the patient's medical history.
📊

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.

⚠️ When to Consult a Doctor:

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

TestFactor V Mutation Screening (F5 - G1691A)Prothrombin Gene Mutation TestAntithrombin III Activity TestProtein C and S Assay
ComparisonFactor 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?
It is a genetic test that detects the G1691A mutation in the Factor V gene, which increases the risk of blood clots.
Why is this test done?
To identify individuals at risk for thrombophilia, especially those with a family history or personal history of blood clots.
How is the test performed?
A blood sample is drawn and analyzed using Real Time PCR to detect the specific mutation.
What does a positive result mean?
A positive result indicates the presence of the mutation, increasing the risk of blood clots. Consult a doctor for management.
What are the risks of the test?
Risks are minimal and include bruising, pain, or rare infection at the blood draw site.
How long does it take to get results?
Results are typically available within 3-4 days after sample collection.
Is fasting required for this test?
No, fasting is not required for Factor V Mutation Screening.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for this test across many cities in India.
What is the cost of the test?
The test costs INR 6000 at DNA Labs India, with home collection included.
Is the test covered by insurance?
Coverage depends on your insurance policy. Check with your provider for details.
What should I do if I have a family history of blood clots?
Consult a healthcare provider to discuss testing and potential preventive measures.
How accurate is the test?
The test is highly accurate for detecting the G1691A mutation, but results should be interpreted clinically.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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