Your DNA predicts.
Your blood confirms.
Upload your DNA file and blood test results. Get a full health report that crosses your genetics with your actual blood markers — confirming which risks are active right now. From €29. No subscription. Made in Europe.
No spam. One email when beta opens. Unsubscribe anytime.
Why this exists
Your DNA already contains the answer. The problem was never the data — it was access, language, and trust.
We built DeepDNA so that understanding your own biology is no longer a privilege reserved for researchers. It is a right you can exercise today.
Every year, adverse drug reactions are among the leading causes of hospital death in Europe.1 Over 95% of us carry pharmacogenomic variants that affect how we respond to common medications.2 A simple test could prevent an adverse reaction.
1 Lazarou et al., JAMA 1998; EMA Pharmacovigilance Reports · 2 CPIC / PharmGKB Consortium · 3 PREPARE Study / European Commission Health Reports
Join the waitlist — limited early access →Your most intimate data
cannot be in foreign hands
In 2025, 23andMe filed for bankruptcy, putting 15 million people's data at risk. Europe's competitive advantage is its values. DeepDNA exists because your genome deserves European-grade protection.
EU-first infrastructure
Your genetic data is primarily processed and stored in European data centers (Germany). GDPR-compliant by design, with EU-first data residency.
Zero data selling. Ever.
We make money from analysis fees, not from your DNA. Your genetic information is never shared with pharma companies, insurers, or any third party.
True delete
One click, everything gone. Raw file, processed results, all derived data. Verified permanent deletion. Not "deactivated" — destroyed.
End-to-end encryption
AES-256 encryption at rest, TLS 1.3 in transit. Per-user encryption keys. Column-level database encryption. Your data is unreadable even to us.
From prediction
to confirmation
Your DNA tells us what could happen. Your blood test tells us what is happening. When you upload both, we cross-reference every genetic finding against your actual blood markers — turning predictions into confirmed, actionable insights. No other service does this.
Your folate factory runs at 30% speed
In a typical analysis, we found the MTHFR gene running at reduced capacity. DNA alone can only predict this might cause issues. But when we crossed it with the blood test:
Consider discussing methylfolate with your doctor as an alternative to regular folic acid — it may be better suited to your genetics. Retest in 3 months. Target: below 10.
Genetic weight risk + perfect metabolism
DNA shows both copies of the FTO appetite gene — a risk factor for obesity. But the blood test reveals perfect glucose, insulin, and HbA1c. Your lifestyle is beating your genetics.
DNA alone is a weather forecast.
DNA + Blood is looking out the window.
What your DNA
already knows
Your genome holds answers that can shape your nutrition, guide which medications you take, reveal inherited risks, and help you plan your family. We make that knowledge yours — not locked in a lab, but alive in your hands.
A plan, not just data
We don't just tell you what's different — we give you personalized insights to discuss with your healthcare provider. Which supplements to explore, suggested dosages, when to retest. Clear next steps, ready for your doctor.
How will your body respond to medications?
Your genes determine how you metabolize drugs. Based on CPIC clinical guidelines with 24+ validated drug-gene pairs. Knowledge that could prevent an adverse reaction — before the first pill.
What good news looks like
Not everything is about risk. Your report also shows everything that came back all clear — blood clotting, iron, diabetes, thyroid. Because knowing what's fine is just as valuable as knowing what to watch.
What does your DNA say about nutrition?
Caffeine metabolism, lactose intolerance, celiac risk, vitamin absorption. Know exactly how your body processes what you eat — backed by your own genetic code, not trends.
See your proteins in 3D
Powered by AlphaFold (Google DeepMind), explore the 3D shape of the proteins affected by your DNA changes. See exactly where in the protein structure your variant sits.
Track your progress over time
Upload new blood tests over time. See which genetic risks are improving or need attention. Your report includes a follow-up calendar with specific targets and dates.
Free to join the waitlist. Pay only when beta launches.
What good news
looks like
We don't just flag risks — we confirm what's working well. Most of your variants are perfectly normal.
From a real DeepDNA report. Your results will reflect your unique genetic profile.
A plan, not
just data
Every report includes a personalized action plan. Not just what your DNA says — what to actually do about it.
Discuss with your doctor
Variants that need medical follow-up — medication adjustments, additional tests, or specialist referrals.
Daily habits
Nutrition, exercise, and sleep adjustments tailored to your genetic profile. Small changes, real impact.
Relax
Variants that came back normal. Nothing to worry about — your body is handling these just fine.
Three clear buckets. You'll know exactly what needs attention, what to tweak, and what to stop worrying about.
The 5-layer pipeline
behind every report
Your DNA file passes through five independent AI and clinical layers before a single finding reaches your report.
Ensembl VEP
Your 720K+ variants are scanned by Ensembl's Variant Effect Predictor. It maps every SNP to genes, transcripts, and proteins — identifying the ones that actually change amino acids.
SIFT + PolyPhen
Two independent algorithms score each protein-changing variant. SIFT uses evolutionary conservation; PolyPhen uses structural and comparative models. Only variants flagged by both advance.
AlphaMissense
Google DeepMind's protein language model assigns a pathogenicity score (0–1) to every missense variant. Trained on primate evolution and protein structure. The final AI verdict.
ClinVar
Each flagged variant is cross-referenced against NCBI's ClinVar — the largest public archive of clinically reported genetic variants and their associated conditions.
AlphaFold 3D
For key findings, AlphaFold renders the 3D protein structure so you can see exactly where your variant sits and how it may affect protein folding and function.
Typical analysis: 720K variants → 2,900 protein-changing → 98 flagged by dual AI → 7 key findings
Already have your 23andMe or AncestryDNA file? Be among the first.
Read My DNA Report — FreeAsk your genome
anything
A conversational AI built into your report. It understands your specific genetic profile and answers in plain language. Powered by the latest genomic research.
Don't lose your spot
Your DNA already has the answers. Let us read them for you.
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See what you'll
actually get
This is a real DeepDNA report. Pharmacogenomics, nutrigenomics, carrier status, polygenic risk scores, traits — and an AI you can ask anything about your results.
Not just risks.
A complete picture
Your report doesn't just flag what to watch — it confirms what's perfectly fine, and gives you an action plan you can start tomorrow.
EVERYTHING THAT CAME BACK ALL CLEAR
YOUR ACTION PLAN — THREE BUCKETS
Bring to your doctor
- Supplements: Consider discussing methylfolate options with your doctor. Get homocysteine tested.
- Vitamin D: Your genetics may influence optimal levels — discuss with your doctor.
- Medications: Share that you're a slow metabolizer before starting new drugs.
Lifestyle tweaks
- Brain care: Exercise, sleep well, stay social, keep learning.
- HDL cholesterol: Aerobic exercise 3-4x/week to raise it.
- Inflammation: Eat colorful, eat omega-3s, manage stress.
Relax about these
- Blood clotting — totally normal
- Iron levels — totally normal
- Diabetes risk — compensated by lifestyle
- Thyroid — all clear
From an anonymized real DeepDNA report. Your report will be personalized to your unique genetic profile and blood markers.
For informational purposes only. This is not medical advice. Consult a healthcare professional before making any health decisions based on genetic data.
One genome.
One lifetime of insights.
Self-knowledge shouldn't be a subscription. Pay once, access forever — because the most important letter you'll ever read shouldn't come with a recurring fee.
No payment now. Join the waitlist and pay only when beta launches. Start with DNA, upgrade to Crossover anytime.
A movement, not just a product
Dare to know
In the 18th century, Kant challenged humanity with two words: Sapere Aude — dare to know. Today, your genome is the ultimate frontier of self-knowledge. Join a generation that chooses knowledge over fear, prevention over reaction, and sovereignty over convenience.
Frequently asked
questions
Everything you need to know before reading your genetic letter.
What is DeepDNA?
What DNA file formats do you support?
Is my genetic data safe?
Is this a medical diagnosis?
How does the AI analysis work?
Can I delete my data?
Stop guessing. Start knowing.
Your DNA already holds the answers about your health, medications, and nutrition. Join the waitlist and be first to read your personal genetic report.