MTHFR C677T/A1298C MUTATIONS DETECTION, EDTA BLOOD

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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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Price: Rs. 8,000.00

Sample Type: EDTA Blood

Fasting Not Required

Notes: M0070

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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Free Sample Pickup from Home/Office

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Need help? Call +91-8595219293

Write FULL NAME for all persons.

Note: Order with incomplete address will be rejected.

  1. Appointment confirmation and Technician details will be provided to you Through Email & SMS well in advance.
  2. The date and time of collection may change if Technicians are not available at the requested time.
  3. Kindly allow 30 minutes (Plus or Minus)for the technician to find and reach your location through possible traffic/weather.

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