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Methylation Genomic

$299.00
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A blue rectangular box labeled "ADHD Genomic" with playful graphics, white clouds, and colorful arrows on a light background. The box hints at personalized ADHD treatment and displays the website plus social media icons on the side.

Methylation Genomic

$299.00

Methylation drives hundreds of essential reactions, from DNA repair to neurotransmitter balance.  This panel identifies variants that may impact methylation efficiency and related pathways. Use your results to inform targeted nutrition and lifestyle strategies that support energy, mood, cardiovascular health, and longevity goals. Results are delivered in the Boomerang Kits App.

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Genetic variants influencing methylation efficiency (MTHFR, COMT, MTRR, and related genes)
Insight into detoxification, mood regulation, and cellular repair processes
Swab collection (buccal)

This panel analyzes genetic variants in the key methylation pathway genes: MTHFR (C677T and A1298C), COMT, MTRR, MTR, and related genes that govern how your body processes folate, regulates homocysteine, and produces neurotransmitters.

Methylation drives over 200 essential cellular reactions — from DNA repair to serotonin and dopamine synthesis. MTHFR variants can reduce enzyme activity by 30–70%, raising homocysteine and impairing active folate production. Understanding your methylation blueprint allows you to target supplementation precisely.

Methylation drives over 200 essential cellular reactions — from DNA repair to neurotransmitter balance. This test reveals how genetic variants impact your methylation cycle, providing insights into fatigue, mood, cardiovascular health, and longevity optimization. Understanding your methylation blueprint empowers proactive supplementation and lifestyle strategies.

MTHFR variants

C677T & A1298C

COMT & dopamine

Neurotransmitter balance

Homocysteine pathway

MTRR, MTR & cardiovascular risk

Nutrition strategy

Methylfolate vs folic acid

Cheek Swab Collection
1
Order Your KitDelivered right to your door.
2
Download the AppRegister your kit with the Boomerang Kits App.
3
Collect Swab SampleUse the sterile swab as instructed to collect your sample.
4
Return MailerPlace the sample in the prepaid envelope and drop it in the mail.
5
Get ResultsView secure results in the app within 24–48 hours after our lab receives your sample.
Is this test right for me?
  • You have been told you carry an MTHFR variant or want to find out if you do (Frosst P et al., Nature Genetics 1995 — MTHFR C677T is one of the most common genetic polymorphisms, present in 10–15% of the population in homozygous form.)
  • You have elevated homocysteine levels and want to understand the genetic cause (Ueland PM et al., Am J Clin Nutr 2000 — MTHFR variants are a primary genetic cause of mild hyperhomocysteinemia, a cardiovascular risk factor.)
  • You experience persistent fatigue, brain fog, or mood issues that haven't responded to standard approaches (Mattson MP & Shea TB, Trends Neurosci 2003 — impaired methylation affects neurotransmitter synthesis, contributing to fatigue, depression, and cognitive difficulty.)
  • You take folic acid and want to know if your body can actually convert it to its active form (Bailey LB & Gregory JF, J Nutr 1999 — MTHFR C677T reduces conversion of folic acid to active methylfolate by up to 70%; methylfolate supplementation may be more effective.)
  • You have a family history of cardiovascular disease, blood clots, or neural tube defects (Homocysteine Studies Collaboration, JAMA 2002 — elevated homocysteine from MTHFR variants is associated with increased CVD and thrombosis risk.)
  • You are pregnant or planning to become pregnant and want to optimize your methylation status (CDC Folic Acid Recommendations; Daly LE et al., BMJ 1995 — MTHFR variants increase neural tube defect risk; methylfolate supplementation is recommended.)
  • You are focused on longevity and cellular health optimization (Ligthart S et al., Nature Comm 2016 — methylation efficiency is linked to biological aging rates and epigenetic clock markers.)
What You're Testing

Key Benefits

Methylation Genomic · Genetic Variant Analysis · Cheek Swab Collection

Panel 01 / METH Genomic Analysis
MTHFRCOMTMTRRMTRFolate CycleMethionine Cycle
Decode Your Methylation Genes
Explore how key genetic variants linked to methylation pathways may influence how your body processes nutrients and supports essential biochemical functions. Results are presented in a clear, structured format to help establish a baseline view of methylation-related patterns involved in energy balance and cellular regulation.
Research Evidence
MTHFR catalyzes the conversion of 5,10-methylenetetrahydrofolate to its active form — the essential step for homocysteine remethylation and a core reaction in DNA synthesis, repair, and epigenetic regulation
The two most common MTHFR polymorphisms (C677T and A1298C) can reduce enzyme activity, disrupt the folate cycle, and lead to elevated homocysteine — an independently validated cardiovascular risk factor
MTHFR, MTR, and MTRR variants play complementary roles in folate metabolism — patients carrying two or more risk genotypes show dramatically higher odds of folate deficiency than those with no risk genotypes
Research Basis
MTHFR polymorphisms are among the most extensively studied genetic variants in clinical medicine. The C677T polymorphism is associated with reduced enzyme activity, increased homocysteine, and elevated oxidative stress — providing a validated mechanistic link between genetic methylation status and cardiovascular and metabolic health.
MDPI Genes 2025 — MTHFR Wide-Ranging Clinical Implications · PMC10779094 · CDC MTHFR Gene Variant Facts
Panel 02 / METH CLIA-certified Lab
DetoxificationNeurotransmitter BalanceDNA RepairCellular RepairHomocysteine Pathway
Understand Core Wellness Pathways
See how key biological pathways linked to methylation support processes like detoxification, cellular repair, and overall system function. Results help organize how these pathways work together, providing a clearer view of how your body manages everyday health processes.
Research Evidence
Methylation drives over 200 essential cellular reactions — COMT is critical for neurotransmitter breakdown, and COMT Val/Met variants produce 30–50% differences in enzyme activity, directly affecting dopamine and norepinephrine clearance
MTHFR and COMT variants together influence homocysteine production and one-carbon metabolism — both variants are associated with elevated homocysteine and cardiovascular disease risk
Impaired MTHFR efficiency can create detoxification and hormone clearance bottlenecks — elevated homocysteine produces reactive oxygen species, contributing to oxidative stress and chronic inflammation
Research Basis
MTHFR is essential for the metabolism of methionine, folate, RNA, proteins, and DNA. Impaired efficiency leads to hyperhomocysteinemia — acknowledged as an independent cardiovascular risk factor, with up to 40% of patients with premature coronary artery disease showing elevated homocysteine levels.
PMC4849464 · COMT 158 Val/Met Variants · PMC10779094 · Oasis Health MTHFR Clinical Reference
Panel 03 / METH Longitudinal Track
Nutrition StrategySupplement ResponseB-Vitamin MetabolismLifestyle PlanningCardiovascular Risk
Personalized Lifestyle Blueprint
See how your genetic markers relate to pathways involved in nutrition processing and daily lifestyle factors. Results are organized to help you better understand how diet and habits may interact with your unique genetic profile, providing a structured reference for personal wellness planning.
Research Evidence
B vitamin supplementation with methylfolate, pyridoxal-5′-phosphate, and methylcobalamin has been shown in an RCT to significantly reduce homocysteine and LDL cholesterol in patients with MTHFR, MTR, and MTRR polymorphisms
The effect of the MTHFR C677T variant on homocysteine is modified by folate status — knowing your genotype helps determine whether methylated forms of B vitamins are the appropriate nutritional strategy
Methylation genetic results are permanent — unlike blood biomarkers, they provide a lifelong framework for understanding individual response to diet, supplementation, and lifestyle interventions
Research Basis
A randomized, double-blind, placebo-controlled trial found that MTHFR, MTR, and MTRR genotype-guided B vitamin supplementation (methylfolate, P5P, methylcobalamin) significantly reduced homocysteine and lipid levels — demonstrating the clinical utility of genetic methylation profiling for personalized cardiovascular risk management.
PMC11173557 · MTHFR/MTR/MTRR RCT, B-Vitamin Supplementation · PMC4555142
CLIA-certified Lab
Cheek Swab Collection
4 Gene Panels
HIPAA Compliant
Secure App Collection
FAQ

Frequently Asked Questions

What's included, how to collect, when you'll see results, and how to use them.

What does this panel measure?

Genetic variants in key methylation-related genes such as MTHFR, COMT, and MTRR that influence detoxification, neurotransmitter balance, and cellular repair.

How is this different from traditional testing?

Boomerang Laboratories applies clinical-grade genomic sequencing and data interpretation to uncover personalized insight into cellular and metabolic efficiency. Your results are presented clearly in the Boomerang Kits App with secure, HIPAA-compliant access.

Who benefits most from this panel?

Individuals optimizing longevity, detoxification, and cellular health, or addressing mood and energy concerns related to methylation efficiency.

How should I use these results?

Share your methylation profile with your clinician or nutrition professional for tailored guidance on nutrient optimization and cellular wellness.

Is this a diagnostic test?

No. This is an informational genomic screening. Results reflect genetic tendencies and should be interpreted alongside lifestyle and clinical factors.

How do I collect the sample?

Collect a simple cheek swab using the provided sterile collection device. Follow the instructions in your insert or app. After collection, place the swab in the provided transport tube, seal it, and mail it back using the prepaid envelope.

How do I return my sample?

Place the sealed swab in the prepaid return mailer and drop it at any postal location.

What if my sample can't be processed?

If your sample is insufficient or damaged, we'll notify you and send a replacement kit at no cost.

How long until I see my results?

Most users receive results within 24–48 hours after the lab receives the sample.

Where do I view my results?

Your results will appear securely in the Boomerang Kits App, under your personalized dashboard.

Is my data private?

Yes. All genomic data is encrypted and stored in secure, HIPAA-compliant systems. Only you can share your results with others.

Is this covered by insurance?

Boomerang Kits are typically not billed to insurance, but HSA/FSA funds may be used depending on your plan.

What other panels complement this one?

GenomeRx Insight for drug metabolism correlations and NAD Longevity Blueprint for cellular performance context.

What does this panel measure?

Genetic variants in key methylation-related genes such as MTHFR, COMT, and MTRR that influence detoxification, neurotransmitter balance, and cellular repair.

How is this different from traditional testing?

Boomerang Laboratories applies clinical-grade genomic sequencing and data interpretation to uncover personalized insight into cellular and metabolic efficiency. Your results are presented clearly in the Boomerang Kits App with secure, HIPAA-compliant access.

Who benefits most from this panel?

Individuals optimizing longevity, detoxification, and cellular health, or addressing mood and energy concerns related to methylation efficiency.

How should I use these results?

Share your methylation profile with your clinician or nutrition professional for tailored guidance on nutrient optimization and cellular wellness.

Is this a diagnostic test?

No. This is an informational genomic screening. Results reflect genetic tendencies and should be interpreted alongside lifestyle and clinical factors.

How do I collect the sample?

Collect a simple cheek swab using the provided sterile collection device. Follow the instructions in your insert or app. After collection, place the swab in the provided transport tube, seal it, and mail it back using the prepaid envelope.

How do I return my sample?

Place the sealed swab in the prepaid return mailer and drop it at any postal location.

What if my sample can't be processed?

If your sample is insufficient or damaged, we'll notify you and send a replacement kit at no cost.

How long until I see my results?

Most users receive results within 24–48 hours after the lab receives the sample.

Where do I view my results?

Your results will appear securely in the Boomerang Kits App, under your personalized dashboard.

Is my data private?

Yes. All genomic data is encrypted and stored in secure, HIPAA-compliant systems. Only you can share your results with others.

Is this covered by insurance?

Boomerang Kits are typically not billed to insurance, but HSA/FSA funds may be used depending on your plan.

What other panels complement this one?

GenomeRx Insight for drug metabolism correlations and NAD Longevity Blueprint for cellular performance context.