MTHFR C677T & A1298C Genetic Mutation Test – DNA Analysis for Methylation & Health Insights
1.000,00 د.إ
The MTHFR C677T & A1298C Detection Lab Test is a genetic screening tool that identifies mutations in the MTHFR gene, which can impact folate metabolism, homocysteine levels, and overall health. Key features include accurate detection of both common MTHFR variants (C677T and A1298C) through a simple saliva or blood sample.
Description
MTHFR C677T & A1298C Genetic Mutation Test – Unlock Your Methylation Potential
The MTHFR C677T & A1298C Genetic Mutation Test from Lab Tests Dubai is a precision DNA screening that identifies two of the most clinically significant variants in the MTHFR (methylenetetrahydrofolate reductase) gene a critical enzyme involved in folate metabolism, methylation, and homocysteine regulation.
These common genetic variations can reduce MTHFR enzyme activity by up to:
- ✅ 70% in homozygous C677T (TT genotype)
- ✅ 40–60% in compound heterozygotes (C677T + A1298C)
When impaired, this leads to:
- Poor conversion of folic acid to active methylfolate (5-MTHF)
- Elevated homocysteine levels (linked to heart disease, stroke)
- Reduced detoxification, neurotransmitter production, and DNA repair
- Increased risk of infertility, recurrent miscarriage, and neural tube defects
This test is essential for:
- Individuals with high homocysteine despite normal folate/B12
- Women experiencing recurrent pregnancy loss or infertility
- Patients with depression, anxiety, or brain fog
- People struggling with chronic fatigue or cardiovascular risks
- Those optimizing health through functional or integrative medicine
Using CLIA-certified PCR or NGS technology, this non-invasive cheek swab or saliva test delivers accurate results within 5–10 business days so you can start supporting your biochemistry with the right form of folate.
Available with home sample collection, Lab Tests Dubai ensures privacy, precision, and proactive care empowering you to thrive at the genetic level.
Why You Need This Test
If you’re taking folic acid but still feel tired, anxious, or unwell, this test could reveal why your body may not be able to activate synthetic folic acid due to an MTHFR mutation.
You need the MTHFR C677T & A1298C Test if:
- You have elevated homocysteine (>10 µmol/L)
- You’ve had recurrent miscarriages or implantation failure
- You suffer from chronic fatigue, depression, or brain fog
- You’re planning pregnancy or undergoing IVF
- You take folic acid supplements but see no benefit
- You have a family history of stroke, blood clots, or early heart disease
This test helps:
- Identify impaired folate metabolism
- Guide use of active folate (5-MTHF) instead of folic acid
- Lower homocysteine naturally with targeted B vitamins
- Support healthy conception and fetal development
- Improve mood, energy, and detox pathways
Symptoms That Indicate This Test
Consider the MTHFR Test if you experience:
✅ For Methylation & Mental Health:
- Chronic fatigue or low stamina
- Anxiety, depression, or mood swings
- Brain fog, poor memory, or difficulty concentrating
- Insomnia or sleep disturbances
✅ For Fertility & Pregnancy:
- Recurrent miscarriages (especially 1st trimester)
- Infertility or failed IVF cycles
- History of preeclampsia or placental issues
- Neural tube defects in previous pregnancies
✅ For Cardiovascular Risk:
- High homocysteine levels
- Family history of stroke or clotting disorders
- Unexplained blood clots (DVT, PE)
These signs may point to impaired methylation and this test helps start the right treatment.
Natural Production: How MTHFR Supports Your Body
The MTHFR enzyme converts:
- Dietary folate and synthetic folic acid → L-methylfolate (5-MTHF)
This active form is essential for:
- ✅ DNA synthesis and repair
- ✅ Neurotransmitter production (serotonin, dopamine, melatonin)
- ✅ Detoxification and hormone balance
- ✅ Lowering homocysteine (high levels damage blood vessels)
Common Genotypes & Impact:
CC (Wild Type) | 100% | Normal function |
CT (Heterozygous C677T) | ~65% | Mild impairment |
TT (Homozygous C677T) | ~30% | High risk of elevated homocysteine |
A1298C (CC/AC/AA) | Moderate impact | Often worsens C677T when combined |
Compound Heterozygote (CT + AC) | ~40–50% | Significant methylation disruption |
What Happens If Untreated? Risks of Ignoring MTHFR Mutations
Ignoring MTHFR dysfunction can lead to:
⚠️ Elevated Homocysteine – increases risk of heart attack, stroke, dementia
⚠️ Pregnancy Complications – miscarriage, preterm birth, birth defects
⚠️ Neuropsychiatric Issues – depression, anxiety, bipolar-like symptoms
⚠️ Chronic Fatigue & Poor Detoxification
⚠️ Misdiagnosis as psychiatric or autoimmune condition
The good news? This is highly manageable with:
- Active folate (L-5-MTHF) – bypasses the genetic block
- Vitamin B12 (methylcobalamin) – supports methylation cycle
- B6 (P-5-P) and Betaine (TMG) – help clear homocysteine
- Lifestyle support (stress reduction, toxin avoidance)
How to Prepare for the Test
To ensure accurate results:
✅ No fasting required
✅ Avoid eating, drinking (except water), smoking, or chewing gum 30 minutes before sample collection
✅ Use the sterile cheek swab or saliva kit provided
✅ Follow the step-by-step instructions for sealing and mailing
Test Overview
Test Name | MTHFR C677T & A1298C Genetic Mutation Test |
Sample Type | Buccal Swab or Saliva |
Methodology | Real-Time PCR or NGS Genotyping |
Turnaround Time (TAT) | 5–10 Business Days |
Category | Nutrigenomics / Molecular Diagnostics |
Purpose | Detect C677T and A1298C polymorphisms affecting folate metabolism |
Testing Location | Lab Tests Dubai – Partnered with CLIA-Certified Labs |
Benefits of the MTHFR C677T & A1298C Test
🔹 Personalizes Folate Supplementation
Stop using ineffective folic acid.
🔹 Reduces Homocysteine Naturally
Protect your heart and brain.
🔹 Supports Healthy Pregnancy
Critical for fetal neural development.
🔹 Improves Mood & Mental Clarity
By fixing methylation at the root.
🔹 Empowers Functional Medicine Plans
Integrate with detox, gut, and hormone protocols.
If you’re tired of feeling foggy, fatigued, or stuck, the MTHFR C677T & A1298C Test gives you the answers you need in 5–10 days.


Symptoms That Indicate This Test


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