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DNA Labs India

Methylenetetrahydrofolate Reductase (MTHFR), Factor V (F5), Factor II (F2) Test

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Methylenetetrahydrofolate Reductase (MTHFR), Factor V (F5), Factor II (F2) Test

Short Name: MTHFR, Factor V, Factor II Test

Also known as: MTHFR Mutation Test, Factor V Leiden Test, Prothrombin Gene Mutation Test, Thrombophilia Panel

Methylenetetrahydrofolate Reductase (MTHFR), Factor V (F5), Factor II (F2) Test test available at DNA Labs India for ₹12,000. Uses End Point PCR, RFLP on Peripheral blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.

OncologyAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify genetic mutations in MTHFR, Factor V, and Factor II genes that may increase the risk of blood clots, heart disease, and pregnancy complications, enabling early intervention and personalized care.

Test Code
3079
Price
₹12,000
Sample Type
Peripheral blood
Result Time
3-4 days
Fasting Required
No
Method
End Point PCR, RFLP
Step 1

Sample Collection

No specific preparation required. Inform your doctor about any medications or supplements.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in your arm by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:No fasting required. Bring doctor's prescription if applicable.
2
During the Test:Blood draw takes about 5-10 minutes.
3
After the Test:Minimal risks; slight bruising may occur.

About This Test

Who Should Get This Test

To identify genetic mutations in MTHFR, Factor V, and Factor II genes that may increase the risk of blood clots, heart disease, and pregnancy complications, enabling early intervention and personalized care.

How to Prepare

  • Ensure proper identification and labeling of the sample
  • Use EDTA vacutainer for blood collection
  • Transport sample at room temperature with cool pack if needed

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"This test is crucial for identifying genetic predispositions to blood clotting disorders, which can inform personalized treatment plans and preventive measures."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral blood
Sample Volume2 ml
ContainerEDTA Vacutainer
Collection MethodVenipuncture

Sample Stability

Room Temperature24 hours
Refrigerated72 hours
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Incorrect sample type or container
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of specific mutations. Consult a healthcare provider for personalized interpretation.
📊

No mutations detected

Low genetic risk for clotting disorders. Maintain healthy lifestyle.

📊

Heterozygous mutation

Moderate risk. May require monitoring or preventive measures.

📊

Homozygous mutation

Higher risk. Consult a specialist for management options.

⚠️ When to Consult a Doctor:

If you have symptoms like swelling, pain, or shortness of breath, or if results indicate mutations, consult a hematologist or genetic counselor.

Limitations

  • Does not detect all genetic variants
  • Results may require confirmation with additional tests
  • Not a diagnostic tool for active clotting events

Risks & Considerations

  • Minor bruising at puncture site
  • Rare infection or dizziness

Interfering Factors

  • Recent blood transfusions
  • Contaminated or hemolyzed samples
  • Improper sample storage

Frequently Asked Questions

What is the MTHFR, Factor V, Factor II test?
It is a genetic test that checks for mutations in genes related to blood clotting and folate metabolism.
Why is this test recommended?
It is recommended for individuals with a history of blood clots, recurrent miscarriages, or family history of clotting disorders.
How is the test performed?
A blood sample is collected and analyzed using PCR and RFLP methods.
Is fasting required for this test?
No, fasting is not required.
What do the results mean?
Results indicate the presence of mutations, which may increase clotting risk. Consult a doctor for interpretation.
How long does it take to get results?
Results are typically available within 3-4 days.
Is home collection available?
Yes, free home collection is available across India.
What is the cost of the test?
The test costs INR 12000.
Are there any risks associated with the test?
The test involves a standard blood draw with minimal risks like bruising.
Can this test diagnose active blood clots?
No, it identifies genetic predispositions, not active clots.
Who should consider this test?
Individuals with personal or family history of thrombosis, pregnancy complications, or cardiovascular issues.
How accurate is the test?
The test is highly accurate for detecting specified mutations, but results should be interpreted by a healthcare professional.
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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Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

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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