MTHFR C677T/A1298C MUTATIONS DETECTION, EDTA BLOOD

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NABL Cap Accredited     
This test detects common mutations (C677T and A1298C) in the MTHFR gene using molecular methods. These mutations can reduce enzyme activity, affecting folate metabolism and homocysteine levels in the body. Identifying these variants helps assess genetic risk associated with thrombosis, cardiovascular disorders, recurrent pregnancy loss, and certain neurological conditions. The test helps clinicians plan appropriate treatment strategies, including nutritional and therapeutic interventions. Blood collected in EDTA is used for analysis.

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  • Free Home Collection

Price: Rs. 8,000.00

Sample Type: EDTA Blood

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What is the purpose of the MTHFR mutation test?
It identifies genetic variants that may lead to elevated homocysteine and increased risk of clotting and pregnancy complications.

Who should consider this test?
Patients with unexplained thrombosis, recurrent miscarriages, high homocysteine levels, or family history of cardiovascular disorders.

Is genetic counseling recommended?
Yes, counseling is helpful to understand clinical significance and inheritance patterns.

Do I need to fast before this test?
No fasting is required.

Can the results affect treatment decisions?
Yes, results may guide supplementation with folate, B12, B6, or other clinical management approaches

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