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MTHFR

MTHFR

A genetic test that identifies mutations in the MTHFR gene, which can affect folate metabolism, methylation, and cardiovascular health. Detects MTHFR gene variants (C677T and A1298C) that influence how the body processes folate and homocysteine—important for heart, brain, and detoxification function.

  • Sample type: Buccal swab or venous blood (home collection supported).
  • Fasting: Not required.
  • Turnaround time: 2–3 weeks.
  • Who it’s for: Individuals with elevated homocysteine, family history of heart disease, infertility, or unexplained fatigue.
AED 2,100.00

This test identifies whether you carry specific MTHFR gene variants (commonly C677T and A1298C) and determines if you are:

  1. Normal (no mutation)
  2. Heterozygous (one copy of the mutation)
  3. Homozygous (two copies of the mutation)
  1. MTHFR C677T
  2. MTHFR A1298C
  1. Fatigue or low energy
  2. Cognitive difficulties or “brain fog”
  3. Cardiovascular issues or high homocysteine
  4. Mood disturbances (anxiety, depression)
  5. Reproductive health challenges

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