Sample report — fictional genotype, real format.

Every gene, status, and recommendation below is exactly how your report will look. Your report is built from your own 23andMe or AncestryDNA raw file.

Sample DNA Supplement Report

The full report for "Sample S." — a fictional profile covering all 9 genetic variants we analyze.

Your Genetic Supplement Profile

Analysis completed on 8/1/2026

folate metabolism

impaired

You may benefit from methylated folate supplements

b12 absorption

normal

Normal B12 absorption and utilization

caffeine metabolism

slow

You may be sensitive to caffeine

vitamin d sensitivity

high

You may need higher vitamin D doses

antioxidant needs

normal

Standard antioxidant requirements

beta carotene conversion

poor

Consider preformed vitamin A

dopamine regulation

slow clearance

Slower dopamine clearance

🍽️ Foods for your genes

Supplements aside — these everyday food choices line up with your variants.

Folate metabolism (MTHFR)

Emphasize: leafy greens (spinach, romaine), lentils & beans, asparagus, avocado, citrus

Go easy on: heavily fortified products that rely on folic acid

Natural food folate is already in forms your body uses directly — helpful when MTHFR variants reduce conversion of synthetic folic acid.

Caffeine (CYP1A2)

Emphasize: earlier-in-the-day coffee or tea, green tea (gentler curve)

Go easy on: afternoon/evening caffeine, energy drinks late in the day

Slower caffeine clearance means the same cup lasts longer — front-load it and sleep will thank you.

Vitamin D

Emphasize: fatty fish (salmon, sardines), egg yolks, fortified milk or alternatives, sensible sun exposure

Your variants are associated with lower vitamin D response, so dietary sources (and testing) matter more than average.

Vitamin A (beta-carotene conversion)

Emphasize: eggs, dairy, fish (preformed vitamin A sources)

Go easy on: relying on carrots/sweet potato alone for vitamin A

Reduced conversion means plant beta-carotene yields less usable vitamin A — preformed sources close the gap. (If pregnant, discuss vitamin A intake with your clinician.)

Steady focus (COMT)

Emphasize: protein at breakfast (eggs, yogurt), green tea instead of a second coffee

Go easy on: big single caffeine hits

COMT variants change how long stimulating neurotransmitters linger — steadier inputs tend to feel better than spikes.

Want this cooked into an actual weekly menu? Food & Absorption (Premium) builds meals around these exact gene-food rules (plus your conditions and allergies).

What stands out in your profile

  • Your two MTHFR results tell one story: C677T (CT) mildly slows folate processing while A1298C came back typical — methylated B-vitamin forms sidestep the slow step entirely.
  • You combine slow caffeine metabolism (CYP1A2) with slow dopamine clearance (COMT) — stimulants hit harder AND stay around longer for you than for most people, so small, early doses fit best.
  • Your VDR variant is associated with a weaker response to vitamin D at standard doses — testing 25(OH)D before and a few months after supplementing shows what your body actually does with it.
  • BCMO1 (CC) means plant beta-carotene converts poorly to usable vitamin A, so preformed sources (eggs, dairy, fish) carry more weight in your diet than they would for most people.

Lifestyle notes

  • Front-load caffeine: keep it to the morning and cap the total — an afternoon coffee can still be circulating at bedtime for your CYP1A2 type.
  • Protein at breakfast and steady meals suit your COMT profile better than big stimulant spikes.
  • Sensible sun exposure plus dietary vitamin D sources (fatty fish, fortified milk) back up your higher vitamin D requirement.
  • Recheck the basics after 8-12 weeks on any new regimen — 25(OH)D, B12 and folate status — and review changes with your healthcare provider.

Ready to see your own genes?

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Your raw DNA file is processed in memory and discarded — only your gene results are saved to your account, and you can delete them anytime.

All genotypes on this page are fictional and for illustration only — no real person's DNA was used. Reports are for educational purposes and are not a substitute for professional medical advice.