Sample · Decode+

See your nutrition & methylation results in Decode+

A real preview of how MTHFR, vitamin D, B12, and other nutrient-related genes are analyzed and turned into a personalized action plan.

Free to start · $59 one-time, lifetime access

What you'll see inside Decode+

Decode+ covers MTHFR, BCMO1, COMT, FUT2, and VDR.

Priority Dashboard

Your top nutrient areas ranked by impact, with the genes and genotypes behind each finding.

MTHFR Compound Callout

If you carry variants in both MTHFR C677T and A1298C, a dedicated callout explains the combined effect on folate metabolism.

Detailed Findings

Each gene analyzed with your genotype, a plain-language explanation, and food-first considerations.

Action Plan

Tiered recommendations organized by priority, with food-first steps you can discuss with your provider.

Lab Tests to Discuss

Suggested blood tests to confirm your genetic findings with real-world nutrient levels.

Scope & Limitations

What Decode+ covers, what it does not, and important caveats about nutrigenomic analysis.

Your nutrition & methylation results — full sample

Sample Data — Not Your Results

DecodeMyBio

Your Nutrition & Methylation Results

Nutrigenomic analysis based on your DNA

Inside Decode+ — sample preview

Your DNA shows 5 nutrient areas to be aware of.

Your Top Nutrient Priorities

1
Folate Metabolismnotable

Mildly Reduced MTHFR Activity (A1298C)

MTHFR A1298C ACMTHFR C677T CT
2
Beta-Carotene Conversionmoderate

Mildly Reduced Beta-Carotene Conversion

BCMO1 A379V CT
3
Catechol-O-Methyltransferase Activitymoderate

Lower COMT Activity (Met/Met)

COMT Val158Met AA
4
Vitamin B12 Absorptionmoderate

Non-Secretor (Reduced B12 Absorption)

FUT2 Secretor Status AA
5
Vitamin D Receptor Functionmoderate

Less Active VDR (FokI ff)

VDR FokI TTVDR BsmI CT

Combined MTHFR Result

You carry variants in both MTHFR C677T (CT) and MTHFR A1298C (AC). This combination is sometimes called compound heterozygous. Published research suggests the combined effect of both variants on folate metabolism may be greater than either variant alone. Each variant individually has a modest effect on MTHFR enzyme activity, but together they can further reduce the enzyme’s ability to convert folic acid into its active form (methylfolate).

This finding is included in the detailed results below. The individual MTHFR C677T and A1298C findings describe each variant separately.

Detailed Results

BCMO1 A379Vmoderate

Trait: Beta-Carotene Conversion

Your Genotype: CT

Result: Mildly Reduced Beta-Carotene Conversion

You carry one copy of the A379V variant. Research suggests this may reduce beta-carotene conversion efficiency by approximately 30%.

Considerations:

  • Consider including preformed vitamin A sources (liver, eggs, dairy) in addition to plant-based carotenoids.

PMID:19103647

COMT Val158Metmoderate

Trait: Catechol-O-Methyltransferase Activity

Your Genotype: AA

Result: Lower COMT Activity (Met/Met)

Your COMT result is Met/Met. You have lower COMT enzyme activity, meaning catecholamines (dopamine, norepinephrine) are broken down more slowly. This is associated with higher baseline catecholamine levels.

Considerations:

  • Support stress management through regular physical activity and adequate sleep.
  • Include magnesium-rich foods: nuts, seeds, and dark leafy greens.

PMID:15166467

FUT2 Secretor Statusmoderate

Trait: Vitamin B12 Absorption

Result: Non-Secretor (Reduced B12 Absorption)

Your FUT2 result indicates non-secretor status.

Full considerations and citations in Decode+

MTHFR A1298Cnotable

Trait: Folate Metabolism

Result: Mildly Reduced MTHFR Activity (A1298C)

You carry one copy of the A1298C variant.

Full considerations and citations in Decode+

MTHFR C677Tnotable

Trait: Folate Metabolism

Result: Mildly Reduced MTHFR Activity

You carry one copy of the C677T variant.

Full considerations and citations in Decode+

VDR FokImoderate

Trait: Vitamin D Receptor Function

Result: Less Active VDR (FokI ff)

Your VDR FokI result indicates the ff genotype.

Full considerations and citations in Decode+

VDR BsmInormal

Trait: Vitamin D Receptor Function

Result: Variant VDR (BsmI Carrier)

You carry one copy of the BsmI variant.

Full considerations and citations in Decode+

Full considerations, food-first recommendations, and citations for all 7 findings in Decode+

Action Plan

Priority 2 — Moderate Findings

  • Consider including preformed vitamin A sources (liver, eggs, dairy) in addition to plant-based carotenoids.
  • Support stress management through regular physical activity and adequate sleep.
  • Include magnesium-rich foods: nuts, seeds, and dark leafy greens.
  • Include B12-rich foods regularly: meat, fish, eggs, dairy, and fortified cereals.

+3 more personalized recommendations in Decode+

Discuss these findings with your healthcare provider or a registered dietitian to determine which steps are most relevant for your situation.

Lab Tests to Discuss

Based on your genetic results, these tests may be useful to discuss with your provider:

  • Homocysteine related to folate and B12 metabolism
  • Serum or RBC folate measures folate status directly
  • Serum B12 measures vitamin B12 levels
  • 25-OH Vitamin D measures vitamin D status

What Decode+ Does Not Cover

  • This is not a diagnosis of any nutrient deficiency or medical condition.
  • This is not a meal plan or personalized dietary prescription.
  • Decode+ does not account for your medications, medical history, or lifestyle factors.
  • Genetics is one input among many that affect nutrient needs — lab results and clinical context matter too.

Important Limitations

  • Nutrigenomics is an evolving field. Research on gene-nutrient interactions continues to develop.
  • Genetic variants are one factor among many that influence nutrient needs. Diet, lifestyle, health conditions, and medications all play a role.
  • These results are for informational purposes only and do not constitute medical or dietary advice.
  • Do not change your diet or supplement regimen based solely on these results. Consult a qualified healthcare provider or registered dietitian.
  • Nutrient status depends on many factors beyond genetics, including absorption, diet quality, and overall health.

This is a sample built from fictional data for demonstration purposes. Your own results in Decode+ reflect your personal genetics.

See your own nutrition & methylation insights

Upload your 23andMe or AncestryDNA raw data. See your genome overview free; unlock your nutrition results with a one-time $59 — yours for life.

Get Started Free

Free vs Decode+

Create your account and see your genome overview free. Decode+ turns your MTHFR, B12, and vitamin D genetics into a structured action plan.

Free to start

  • Create your account & upload 23andMe or AncestryDNA
  • Your genome overview — genes analyzed, variants found
  • Export or delete your data anytime
  • MTHFR and methylation analysis
  • Prioritized nutrient dashboard
  • Food-first action plan

Decode+

$59 one-time
  • Everything in free, plus:
  • MTHFR compound analysis (C677T + A1298C)
  • 7 nutrigenomic genes analyzed
  • Prioritized nutrient dashboard
  • Food-first action plan with provider note
  • Plus medications, carrier status, ancestry & the AI assistant

Personalized Nutrigenomics from DNA You Already Have

Decode+ uses raw data from 23andMe or AncestryDNA — free to start, then a one-time $59 you own for life. Clinical nutrigenomic panels ordered through functional medicine providers can cost $200 or more and often require a new sample.

Decode+ covers MTHFR, B12 absorption, beta-carotene conversion, vitamin D receptor function, and more — with food-first recommendations you can act on or discuss with your provider.

Evidence-Based Nutrigenomics

Every finding cites peer-reviewed research. Gene-nutrient associations are drawn from published studies and cross-referenced with your genotype data.

For educational and informational purposes only. Not a substitute for clinical testing or medical advice. See our limitations page for details.

Ready to See Your Nutrition Insights?

Upload your 23andMe or AncestryDNA raw data and read your results inside Decode+. Free to start — then $59 one-time, yours for life.

Medical Disclaimer

DecodeMyBio provides informational pharmacogenomic insights only. This is not medical advice. Always consult your healthcare provider before making medication changes.