Sample report— synthetic genetic data for demonstration only
Get Your Report — $99This report has not been evaluated by the FDA. It is for educational and informational purposes only. It is not intended to diagnose, treat, cure, or prevent any disease. Not a substitute for professional medical advice. PeptidesDNA is not a medical practice, pharmacy, or healthcare provider. Consult a qualified healthcare provider before making any health-related decisions.
Sample Report · What you receive
Your Genetic
Peptide Analysis
This is a sample of the full report you receive after uploading your DNA. Every section below is built from your own genetics, scored across 27 peptide compounds.
94
Markers found
of 120 targets
27
Peptides scored
compounds
94
Top match
out of 100
78%
Data coverage
26 missing
Your DNA tells a clear story.
Three genes do most of the work in shaping how your body responds to peptides — your stress chemistry, your tissue repair signal, and your methylation engine. Here is what we found, in plain language.
Balanced dopamine — sharp under pressure, but slow to come back down
COMT · rs4680 Val/Met
Upside
Faster information processing, solid working memory, strong analytical edge in calm conditions.
Watch out
Dopamine clears slowly under stress — anxiety lingers in the body longer than average. Peptides that modulate dopamine (Semax) ranked high in your report for this reason.
Reduced activity-dependent BDNF — neuroplasticity needs a push
BDNF · rs6265 Val/Met
Upside
When you do learn, it sticks. Strong consolidation, durable memory traces.
Watch out
Lower baseline BDNF means you need more deliberate stimulation — exercise, fasting, novelty — to drive new growth. Semax directly upregulates BDNF and addresses this exact gap.
Intermediate methylation — moderate folate processing
MTHFR · rs1801133 C677T (C/T)
Upside
Mid-tier folate conversion. Not the worst phenotype, not the best. Methylated B-vitamins fully restore function.
Watch out
Affects glycine and SAMe availability, both of which feed into peptide synthesis pathways. We adjusted protocol pacing to account for this.
Beyond your brain
Soft tissue
Vulnerable
COL5A1 + MMP1 variants elevate connective tissue turnover. BPC-157 is your single highest-confidence match for this reason.
Lactose
Tolerant
LCT rs4988235 T/T — lactase persists into adulthood. Dairy will not disrupt your gut peptide protocol.
Exercise response
Strong
ACE rs4343 G/G + favorable NOS3 baseline. Your cardiovascular response to exercise is above average — zone-2 cardio will pair well with the protocol.
Significant finding
Cardiovascular9p21 region — moderate cardiovascular risk variants detected
Three variants in the 9p21 region (rs10757274, rs2383206, rs1333049) are heterozygous. This region is the single strongest population-level signal for coronary artery disease risk. Peptides that affect blood pressure or coagulation (PT-141, CJC-1295) should be approached cautiously and discussed with your physician before use.
Inflammation profile
IL6 rs1800795 G/C + TNF rs1800629 G/A — your baseline inflammatory tone runs moderately high under stress. This is the underlying reason GHK-Cu and BPC-157 ranked meaningfully above the population average in your scoring.
Anti-inflammatory peptides (GHK-Cu, KPV, Thymosin Alpha-1) will likely work harder for you than for the average user.
Vitamin D
Likely deficient
GC rs2282679 A/C — reduced vitamin D binding protein. Your serum 25(OH)D is likely 20–30% lower than your sun exposure would suggest.
Test 25(OH)D. Supplement 2,000–4,000 IU daily with K2.
Vitamin A
Slow conversion
BCMO1 rs7501331 T/T — your body converts beta-carotene to retinol about 50% less efficiently than average. Plant sources alone may not meet baseline.
Favor pre-formed retinol (animal sources or a supplement) over beta-carotene.
Sleep & Circadian
Mild evening chronotype
PER3 + CLOCK variants suggest you run as a mild night owl. Cortisol peaks roughly 90 minutes later than average. Schedule peptides accordingly.
Push the BPC-157 morning dose to 7–8 AM instead of 6. Take Semax at 9 PM, not 10.
How your methylation affects peptides
You are a moderate methylator. MTHFR C677T heterozygous + MTRR rs1801394 A/G means methylation runs at about 70% of population baseline. This affects how your body processes peptides that interact with the SAMe cycle, as well as your sensitivity to specific co-factors.
Methylated B-vitamins recommended
Use methylfolate (5-MTHF) and methylcobalamin (B12) instead of folic acid and cyanocobalamin. This supports the peptide synthesis pathways your DNA partially under-resources.
Glycine demand is elevated
BPC-157 metabolism is glycine-dependent. Bone broth or 5 g of supplemental glycine daily before bed supports the protocol meaningfully.
Space high-dose niacin from peptides
Niacin above 500 mg depletes methyl groups in real time. Separate from any peptide dose by at least four hours.
Avoid during peptide protocols
Pathway scores
How your genetics score across six biological systems. Higher = stronger genetic signal for peptides targeting that pathway.
Tissue Repair
Strong
Inflammation
Elevated
Gut Integrity
Strong
GH / IGF-1 Axis
Above avg
Neuroprotection
Strong
Longevity
Above avg
Your peptide matches
Based on your profile, here's what your genetics suggest.
Each compound scored 0–100 against your genetics. Tap any peptide to see your specific markers and reasoning.
Your Markers
Why this ranks here
Moderate-HighThree of your strongest variants converge on connective tissue: collagen turnover, matrix breakdown, and TGF-β signaling. BPC-157 directly stimulates each pathway. This is your single highest-confidence match.
What this means for you
Recovery from joint, tendon, and ligament strain will respond meaningfully to BPC-157 — likely above-average effect vs. the population mean. Expect noticeable change in soft-tissue healing within three to four weeks.
Dose
400 mcg/day
Stacking
Pairs with GHK-Cu (#2) for surface + structural repair. Add TB-500 (#7) for tendons specifically.
Not approved by any regulatory agency. No completed human clinical trials. Dosing based on animal PK data and practitioner protocols.
2 peptides may benefit from lower starting doses.
We checked all 27 peptides against your seven CYP enzymes and your genetic profile. Two peptides need adjusted starting doses because of your intermediate CYP2D6 phenotype.
CYP2D6 intermediate — start at half-dose and titrate up
CYP2D6 intermediate — half-dose start
All other 8 peptides: standard dosing
Most peptides are broken down by peptidases, not CYP liver enzymes. Your CYP profile doesn't affect their dosing. Each peptide card above shows its specific dose.
Which combos work. Which don't.
Based on known pharmacological pathways, we flagged potential interactions between your top compounds. This is not a comprehensive interaction check — consult your healthcare provider.
Classic complementary stack — structural + surface repair. No pathway overlap or competition.
GLP-2 supports gut barrier; BPC-157 supports systemic tissue. Synergistic for digestive recovery.
Both target fat metabolism through different mechanisms. Can stack, but space doses by ≥4 hours and monitor blood glucose closely.
Both modulate central neurotransmitters with overlap. Risk of overstimulation. If using both, separate cycles by ≥1 month.
Canonical recovery stack. No pharmacological conflict. Frequently used together in tendon protocols.
Selank's anxiolytic effect may mask early hypoglycemia warning signs. Monitor glucose carefully if combining.
When you take it matters as much
as what you take.
We built a daily schedule that aligns each peptide with your body's natural rhythms.
Morning
6:30–8:30 AM (shifted later for your chronotype)
Take with first meal. Aligns with cortisol peak — tissue repair signal is highest in the morning.
Gut barrier activity is highest pre-meal. Take 20 minutes before breakfast.
Midday
12:00–1:00 PM
Lunch-break application — skin and surface tissue. Avoid direct sunlight for 30 minutes after.
Evening
6:00–7:00 PM
Twice-weekly cadence. Post-workout aligns with the repair cascade.
Night
9:00–10:00 PM (90 minutes before bed)
Half-dose for your CYP2D6. Promotes memory consolidation during sleep — do not take after 10 PM (insomnia risk).
A suggested approach in three phases.
Establish gut + baseline repair
Start by reinforcing gut absorption and systemic tissue baseline. GLP-2 first raises uptake of everything that follows. BPC-157 begins addressing your collagen turnover signature.
Add tissue + metabolic
Layer GHK-Cu for surface repair and elastin support. If pursuing metabolic optimization under physician care, Semaglutide is predicted to respond favorably to your GLP1R variant.
Cognitive layer + recovery scale-up
Add the cognitive layer for sustained focus. TB-500 reinforces tendon-specific repair. Re-evaluate biomarkers at week 12 before cycling.
5 markers weren't on your chip
23andMe was built for ancestry, not pharmacogenomics. Your report is still valuable with the 94markers we found — these missing ones would refine scores, not change the overall picture.
Leptin signaling variant — would refine Semaglutide and AOD-9604 scores by roughly five points either direction.
Affects: Semaglutide, AOD-9604 · rs7799039
Angiotensinogen — important for blood-pressure-pathway peptides. Not critical for your current top 10.
Affects: PT-141, blood pressure pathway · rs5051
Bone density signaling — relevant for IGF-1 axis peptides if you choose to layer those in later.
Affects: CJC-1295, Sermorelin · rs3736228
Adrenergic receptor — affects stimulant peptide response (Semax, Selank).
Affects: Semax, Selank · rs28365031
Caffeine sensitivity
Slow
CYP1A2 *1F/*1F variant — you clear caffeine about 30% slower than average. Keep your last coffee before noon for clean peptide nights.
Alcohol metabolism
Normal
ADH1B + ALDH2 standard variants. No flushing reaction expected. No specific interaction concern with peptide protocols.
Saturated fat sensitivity
Moderate
APOE ε3/ε3 — average lipid response to saturated fat. A Mediterranean-pattern diet pairs well with any peptide protocol.
Your liver enzymes & peptide dosing
Most peptides bypass your liver entirely — they're broken down by peptidases, not CYP enzymes. But a few peptides that affect dopamine and hormones are influenced by your CYP profile. This panel is also useful context for your doctor for any prescription medications. This should not be used to start, stop, or change any medication.
About this report
This is not medical advice. This report has not been evaluated by the FDA. It is for educational and informational purposes only. It is not intended to diagnose, treat, cure, or prevent any disease. It is not a substitute for professional medical advice, diagnosis, or treatment. PeptidesDNA is not a medical practice, pharmacy, or healthcare provider.
Consult your healthcare provider. Any dosage decision should be made by or in consultation with a qualified healthcare provider. Dosage ranges shown are from published research and practitioner protocols — they are not prescriptions. Do not start, stop, or change any medication based on this report.
Evidence varies. Scores reflect pathway-level inference from published research, not clinically validated diagnostic results. The strongest pharmacogenomic data exists for GLP-1 receptor agonists. For most other peptides, genetic matching is based on pathway-level inference. Most peptides discussed are not FDA-approved drugs. Availability and legal status of peptides varies by jurisdiction.
Interactions are not comprehensive. The interaction flags in this report are based on known pharmacological pathways. This is not a comprehensive drug interaction check and does not replace consultation with a pharmacist or physician regarding potential interactions with your current medications.
Your report. Your DNA.
This is what you get.
Built from your own genetics.
Upload your 23andMe / AncestryDNA file or order a saliva kit. Your full report in 24–48 hours.
No subscription. Lifetime access. Delete anytime.