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F2 Gene Thrombophilia due to thrombin defect NGS Genetic Test

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F2 Gene Thrombophilia due to thrombin defect NGS Genetic Test

Short Name: F2 Gene Thrombophilia NGS Test

Also known as: Prothrombin Gene Mutation Test, F2 Gene Sequencing Test, Thrombophilia Genetic Panel

F2 Gene Thrombophilia due to thrombin defect NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to diagnose genetic thrombophilia caused by F2 gene mutations, assess the risk of blood clot formation, guide treatment decisions, and enable family screening for hereditary clotting disorders.

Test Code
2698
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Inform the healthcare provider about any medications or recent medical procedures.

Method: Venipuncture or Fingerstick

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm or a fingerstick for FTA card collection. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bruising. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Provide clinical history and undergo genetic counseling as recommended.
2
During the Test:Blood sample collection via venipuncture or fingerstick.
3
After the Test:Wait for report delivery in 3-4 weeks and discuss results with your doctor.

About This Test

Who Should Get This Test

The purpose of this test is to diagnose genetic thrombophilia caused by F2 gene mutations, assess the risk of blood clot formation, guide treatment decisions, and enable family screening for hereditary clotting disorders.

How to Prepare

  • Ensure proper identification and labeling of the sample
  • Use sterile equipment for blood collection
  • Store samples at ambient temperature as specified

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for F2 gene mutations is essential for diagnosing hereditary thrombophilia, guiding preventive strategies, and managing blood clot risks in affected individuals."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL
ContainerEDTA Tube or FTA Card
Collection MethodVenipuncture or Fingerstick

Sample Stability

Blood in EDTA tube: Stable for 7 days at 2-8°C
FTA Card: Stable at room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the F2 gene associated with thrombophilia. Positive results suggest an increased risk of blood clots, while negative results indicate no detected pathogenic variants.
📊

No pathogenic variant detected

Low genetic risk for F2-related thrombophilia. Clinical correlation recommended.

📊

Pathogenic variant detected (e.g., Prothrombin G20210A)

Increased risk of thrombosis. Consult a hematologist for management strategies, including anticoagulation therapy.

⚠️ When to Consult a Doctor:

Consult a hematologist or genetic counselor if you have a positive result, family history of clotting disorders, or symptoms of thrombosis for personalized risk assessment and management.

Limitations

  • May not detect all rare or novel F2 gene variants
  • Does not assess acquired thrombophilia factors
  • Results require clinical correlation and genetic counseling

Risks & Considerations

  • Minor bruising or discomfort at the blood draw site
  • Rare risk of infection or fainting

Interfering Factors

  • Contaminated or degraded DNA samples
  • Recent blood transfusions affecting DNA analysis
  • Technical errors in sample collection or processing

Frequently Asked Questions

What is the F2 Gene Thrombophilia NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to identify mutations in the F2 gene, which can cause thrombophilia due to thrombin defects, increasing the risk of blood clots.
Who should consider this test?
Individuals with a family history of thrombophilia, personal history of unexplained blood clots, recurrent miscarriages, or symptoms like leg swelling and shortness of breath.
What is the cost of the test?
The test costs INR 20000.0 at DNA Labs India, with home sample collection available across India.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to sequence the F2 gene for mutations.
Is fasting required for this test?
No, fasting is not required for the F2 Gene Thrombophilia NGS Genetic Test.
What sample types are accepted?
Blood, extracted DNA, or one drop of blood on an FTA card are accepted samples.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do positive results mean?
Positive results indicate a mutation in the F2 gene, suggesting an increased risk of thrombophilia and blood clots. Consult a doctor for management.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What are the symptoms of F2 Gene Thrombophilia?
Symptoms include pain and swelling in the legs, shortness of breath, chest pain, coughing up blood, blurred vision, and severe headache.
How is thrombophilia diagnosed?
Diagnosis involves genetic testing like this NGS test, along with clinical evaluation and other coagulation tests as recommended by a hematologist.
What should I do after receiving the test results?
Discuss the results with a healthcare provider or genetic counselor to understand the implications and plan preventive measures or treatment.
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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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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