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Factor V Leiden Mutant Detection (G1691A Mutation)

Also referred as
Factor V Leiden Mutation Test
+2
G1691A Mutation Test
Factor V R506Q Mutation Test
For men & women
Earliest reports in
192 hours
Contains
1 test
Test price:
₹5399
₹5900
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The Factor V Leiden Mutant Detection (G1691A Mutation) test is a blood test that identifies the presence of a specific genetic mutation called factor V Leiden. This mutation can increase the risk of abnormal blood clot formation, helping doctors evaluate the likelihood of venous thrombosis and related conditions.

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Blood
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NABL accredited partner lab
This is an outsourced test. The sample for this test is collected by Tata 1mg and processed at a NABL-accredited partner lab.
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Understanding Factor V Leiden Mutant Detection (G1691A Mutation)

Factor V is a protein that plays a central role in blood clotting. Normally, activated protein C regulates clot formation by inactivating factor V to prevent excessive clotting. However, a mutation in the factor V Leiden gene (G1691A) makes the factor V protein resistant to being inactivated, which can lead to a higher risk of developing abnormal blood clots, such as deep vein thrombosis (DVT) or venous thromboembolism (VTE).

Identifying the presence of the Factor V Leiden mutation is important because it helps explain why some individuals are more prone to abnormal clotting. 

The Factor V Leiden Mutant Detection (G1691A Mutation) test is especially useful for individuals with unexplained or recurrent episodes of blood clots, including deep vein thrombosis (DVT) or venous thromboembolism (VTE). It is recommended for patients with a personal or family history of the factor V Leiden mutation or those with a family background of blood-clotting disorders. Women experiencing recurrent miscarriages or pregnancy complications linked to abnormal clotting may also benefit from this test, as the mutation can contribute to pregnancy loss. In addition, it is valuable in cases of clinically suspected thrombophilia, where an inherited gene mutation may increase the risk of abnormal clot formation. By identifying whether a person carries the factor V Leiden mutation, doctors can assess the risk of thrombosis and guide appropriate preventive measures and treatment strategies.

No special preparation is needed for getting the Factor V Leiden Mutant Detection (G1691A Mutation) test done. However, it is preferred that you share your clinical history, current medications, and supplement use with your doctor before giving the sample, as these may influence the results.

Test result ranges are approximate and may differ slightly between labs depending on the methodology and laboratory guidelines. Do not self-medicate, and always consult a doctor to understand the test results correctly. 

Please note: This is an outsourced test. The sample for this test is collected by TATA 1MG and processed at a NABL accredited partnered lab.

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What does Factor V Leiden Mutant Detection (G1691A Mutation) measure?

The Factor V Leiden Mutant Detection (G1691A Mutation) test determines whether a person carries the specific genetic change in the factor V gene known as the G1691A mutation. This mutation alters the way factor V functions by making it resistant to inactivation by activated protein C (APC), a natural regulator that normally helps control clot formation. When factor V cannot be properly switched off, the balance between clot formation and breakdown is disrupted, leading to an increased tendency for abnormal blood clots to develop in the veins.

By detecting the presence or absence of this mutation, the test helps doctors determine an individual’s inherited risk of venous thrombosis, including deep vein thrombosis (DVT) and venous thromboembolism (VTE). It also provides useful information for patients with a family history of clotting disorders or those with unexplained episodes of thrombosis. Identifying this genetic risk factor allows healthcare providers to recommend preventive measures, lifestyle modifications, or medical treatment to reduce the likelihood of future clot-related complications.

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Factor V Leiden Mutant Detection (G1691A Mutation) test price for other cities

Price inMumbaiRs. 5539
Price inBangaloreRs. 5849
Price inNew DelhiRs. 6600
Price inPuneRs. 5599
Price inHyderabadRs. 5610
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FAQs related to Factor V Leiden Mutant Detection (G1691A Mutation)

It is a blood test that looks for a specific genetic mutation (G1691A) in the factor V gene, which increases the risk of abnormal blood clots.
The test is done to check if you have inherited the factor V Leiden mutation, which can make you more likely to develop conditions like deep vein thrombosis (DVT) or venous thromboembolism (VTE).
This test is advised if you have unexplained blood clots, a family history of clotting disorders, recurrent miscarriages, or if your doctor suspects thrombophilia.
A small blood sample is taken from a vein and analyzed in the lab using real-time PCR technology to detect the mutation.
No, fasting is not required for this test.
A positive result means the factor V Leiden mutation is present, which increases your risk of developing blood clots.
Yes, some people carry the mutation but may never develop clots. However, their risk is higher compared to people without the mutation.
A negative result means you do not carry the factor V Leiden mutation, and your risk of inherited thrombophilia from this mutation is low.
Yes, the factor V Leiden mutation is passed from parents to children. You can inherit one or two copies of the mutated gene.
Having one copy (heterozygous) increases your risk moderately, while having two copies (homozygous) increases your risk of clotting much more.
Yes, it is useful in cases of recurrent miscarriages or pregnancy problems linked to abnormal clotting.
The mutation itself cannot be cured, but its risks can be managed with proper medical care and preventive measures.
Tata 1mg ensures accurate lab test results through certified laboratories that use advanced technology and adhere to stringent quality control measures. This commitment to high standards guarantees reliable results.
Recommended for everyone
This package is designed with everyone’s overall health considerations in mind, offering assessments to address a wide range of wellness needs.
Package can be booked by :
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Contains 1 test
Factor V Leiden Mutant Detection (G1691A Mutation)
Report delivery
Standard time
192 hrs
For slots after 11 AM, report will be delivered in 216 hours.
Samples required
Blood
Our phlebotomist will draw a blood sample, typically from a vein in your inner elbow.
Preparations
1
Clinical history is preferred.
Why is this test booked?
1
To identify individuals with an increased risk of venous thrombosis
2
To detect if a patient has an inherited gene mutation that predisposes them to blood clots
3
In cases of clinically suspected thrombophilia
4
When there is a family history of the factor V Leiden mutation
5
To guide preventive strategies and treatment in individuals at risk of clotting disorders
6
In medical conditions, such as recurrent miscarriages or unexplained thrombosis
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