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Free Methylation DNA Panel

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Explore seven genetic markers across MTHFR, MTRR, MTR, TCN2, COMT, and MTHFD1 using your raw DNA file. See your genotypes with short explanations covering folate metabolism, vitamin B12 pathways, and related methylation processes.

 

Your DNA file is processed in your browser. Your raw DNA file and individual genetic results are not uploaded to our servers during analysis. Learn more about privacy and security.

Gene & Variation
Your Genotype
Result
Interpretation

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We support raw DNA files from:

  • 23andMe

  • AncestryDNA

  • MyHeritage

  • FamilyTreeDNA

  • LivingDNA

  • TellmeGen

  • Other major providers

Processed in your browser only.

Your data is never uploaded

or stored.

Which Markers Are Included?

The panel checks these seven markers in your file:

MTHFR: C677T and A1298C — rs1801133 and rs1801131
MTRR: A66G — rs1801394
MTR: A2756G — rs1805087
TCN2: C776G — rs1801198
COMT: Val158Met — rs4680
MTHFD1: G1958A — rs2236225

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Coverage varies between DNA providers and testing versions. A missing result does not mean you have the typical genotype.

Learn how we select and interpret genetic markers.

Methylation Panel Overview

​This panel highlights selected genetic markers involved in folate metabolism, vitamin B12 transport and recycling, homocysteine pathways, and methylation-related processes.

Methylation is an essential biological process involved in many core functions in the body.

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This analysis is based on your raw DNA data and focuses on commonly discussed genetic variations that may influence how efficiently certain pathways operate.

How to Read Your Results

Each result is categorized using a simple system:

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  • 🟢 Typical (--)
    You carry two copies of the allele classified as typical for this marker.

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  • 🟡 Heterozygous (+-)
    You carry one common and one variant copy. This may moderately influence how your pathway functions.

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  • 🔴 Homozygous variant (++)
    You carry two variant copies. This may have a stronger influence on the related biological process.

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These labels describe your genotype, not a severity score. The significance varies by marker, and two variant copies do not always mean a stronger effect. Read the interpretation alongside each result.

Explore More of Your DNA

Continue exploring with GeneExplorer’s free DNA insights, or browse our DNA reports and tools to see what else GenesUnveiled offers.

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Looking for broader access? Compare membership options.

Want more?

​​GenesUnveiled provides:

  • 170+ Health & Gene Reports

  • 80+ Traits & Response Markers

  • 185+ Additional DNA Insights

  • Smart Summary with 150+ Insights​​

  • ​SNP Lookup Database

Genetic risks for heart disease and psychosis on a methylation panel.

Disclaimer

  • This panel is for informational purposes only and does not measure your current methylation status.

  • Results should be interpreted as general tendencies, not definitive outcomes.

  • Not all possible genetic markers are included.

  • If a marker is not shown, it means it was not found or not available in your data.

GenesUnveiled

We provide the tools you need to unlock the potential of your raw DNA file – with 425+ personalized reports, and more on the way. ​GenesUnveiled offers information for informational and educational purposes alone. Nothing on GenesUnveiled is intended to treat, diagnose or cure any conditions.

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