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What your raw DNA file says about your health, without uploading it.
Open the raw data export you already have from 23andMe, AncestryDNA or MyHeritage. Full Human reads it on your device and writes a 17-section PDF: the risk variants you carry, how strong each effect is, and the PubMed study behind every row. Your genome never reaches our servers.
Works with files from 23andMe · AncestryDNA · MyHeritage · FamilyTreeDNA · Living DNA · WeGene
Not sure your file is the right one? Check it here, no account needed →
- 0 bytes
- of DNA data sent to our servers
- 1,114
- conditions and traits in the catalog, 17 sections
- 1,459
- peer-reviewed studies, each linked from your PDF
- No subscription
- pay per PDF; failed generations refunded
Data: NHGRI-EBI GWAS Catalog, release June 2026 · Payments by Stripe · Governed by Swiss law · Failed generations refunded automatically
02 — Inside your report
For each condition: a verdict, the evidence, and the study behind it.
01
A verdict per condition
Higher, lower or average risk, from the risk alleles your file shows you carry. When your file lacks the variants studied for a condition, the report says so instead of guessing.
02
The evidence table
rsID · risk allele · your genotype · odds ratio or beta · PubMed ID. One row per variant, so you or your doctor can check every claim.
03
Plain-language context
What each condition is and what the literature says about prevention, in English, German or French.
Fig. 2 — Some of the conditions covered
Coronary artery disease · Atrial fibrillation · Celiac disease · Psoriasis · Ulcerative colitis · Rheumatoid arthritis · Crohn's disease · Gout · Breast cancer · Prostate cancer · COPD · Major depression · and many more
Associations from published studies, not diagnoses. Effects are combined without correction for correlated variants. How the score is built →
03 — How it works
Three steps. Your file stays on your side of the line.
Step 1
Download your raw file
Export the raw DNA data from your testing provider. Step-by-step guide →
Step 2 · On your device
Open it in your browser
Our generator runs locally (WebAssembly). The file is read in memory and never uploaded.
Step 3
Download your PDF
Save it, keep it, share it with your doctor. We never see it and can't recover it.
Your device
Our servers only see
Your account, credit balance, payments (Stripe) and which report type was generated. No DNA. No report contents.
04 — Reports
One complete report, or just the chapter you care about.
Every category
Complete health report
All health categories in one PDF: risk alleles, your genotype, effect size (odds ratio or beta) and PubMed references for each condition.
Separate report
Nutrition report
How your variants relate to nutrition-related traits, with the same sourcing as the health report.
17 category reports
Each category is also available as its own short PDF · 1 credit
All 17 categories are included in the complete health report.
- 01Autoimmune & inflammatory
- 02Cancer
- 03Cardiovascular
- 04Congenital
- 05Dental & oral health
- 06Dermatological
- 07Endocrine & metabolic
- 08Gastrointestinal
- 09Genetic & metabolic
- 10Infectious diseases
- 11Musculoskeletal
- 12Neurological & mental health
- 13Obstetrics & gynecology
- 14Other conditions
- 15Reproductive
- 16Respiratory
- 17Urological
05 — Pricing
$5.00 per PDF. No subscription.
Buy report credits in packs of 1, 5, 10 or 20. A credit is only used once your PDF is generated; if generation fails, it's refunded automatically. Unused credits stay in your account and work for any family member's file too.
Your DNA kit cost far more than this. The health report it never came with is $5.00.
For comparison: Promethease charges $25 per report and needs your file uploaded (prices checked October 2026).
06 — Guides
Start here
Guides · 10 min read
How to Download Your Raw DNA Data From 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA and WeGene (2026)
Guides · 11 min read
How to Read a DNA Health Report: SNPs, Genotypes, Risk Alleles, Odds Ratios and the Verdict
Comparisons · 10 min read
Promethease Review 2026: What It Is, What It Costs, and the Alternatives
Who makes this
Two people, no lab, no data business.
Full Human Health is built by Floriel Fedry, software engineer and author of PurgeCSS, and Michèle Pfister, co-founder. We built it because the only way to be sure a DNA file stays private is never to receive it.
About Full Human Health →
Floriel Fedry
Co-founder & software engineer · author of PurgeCSS, creator of Orphos
Michèle Pfister
Co-founder · health innovation and personalized medicine
07 — Questions
Before you start
Reports are informational and are not a medical diagnosis. Talk to a qualified professional before acting on genetic results.
- Which DNA testing services are supported?
- You can use compatible DNA files from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA, and WeGene.
- Is my data secure?
- Your DNA file is analyzed entirely in your browser, and your report PDFs are created on your device. Neither is uploaded to or stored on our servers. We store account, payment, credit balance, and generation status records to operate the service, but no DNA data or report contents.
- How accurate is the report?
- Every row is a published genome-wide association from the NHGRI-EBI GWAS Catalog, with its PubMed ID so you can read the study. The verdict per condition combines the effects of the risk alleles you carry; it does not correct for correlated variants and is not a clinical polygenic risk score. Treat 'higher risk' as a prompt to talk to a doctor, not as a diagnosis.
- What do higher, lower and average risk mean?
- They compare the combined effect of the risk alleles you carry with carrying none. 'Average or undetermined' means the effects balance out, or your file does not include the variants studied for that condition.
- Which conditions are covered?
- Hundreds of conditions in 17 sections, from coronary artery disease and atrial fibrillation to celiac disease, psoriasis and rheumatoid arthritis, plus a separate nutrition report. The sample report shows how a complete report is organized.
- How long does it take to get results?
- Reports are generated in your browser and downloaded as PDFs when ready. Processing time depends on your device and the selected reports. Keep the page open while generation runs; reports are not sent by email.
- I don't have a raw DNA file yet.
- You need the raw data export from a consumer test: 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA or WeGene. If you have tested, the export takes a few minutes — follow our guide. We don't sell kits and never see your sample.
- Is Full Human Health free?
- No. Each PDF costs one credit and there is no subscription. The sample PDF is free and shows exactly what a report contains.
- Why does a complete report cost so little?
- Your DNA is processed by your own computer, not by our servers. There is no lab, no cloud computing per report and no stored data to pay for, so we charge for the software and the curated catalog, once per PDF.
- How is this different from Promethease or 23andMe's own reports?
- 23andMe interprets its own test on its servers. Promethease needs your file uploaded and returns a long list of SNPedia entries for $25. Full Human reads the file you already have, on your device, and writes a readable PDF organised by condition, with the study behind every row, for the price of one credit.
- Can I use one account for my family's DNA files?
- Yes. Credits are not tied to a file: pick any raw file for each report. Parents, partners and siblings can each get their own PDF from one account, with their permission, and nothing is uploaded for any of them.
- Does it work on a phone?
- Generation runs inside the browser tab and needs memory, so a laptop or desktop is the reliable choice. Keep the tab open until your PDFs have downloaded.
- What if generation fails?
- A credit is only used after a valid PDF is produced. Failed or abandoned generations are refunded automatically.
- Can I get a refund?
- A failed generation refunds its credit automatically. Credit purchases are otherwise final; write to support@full-human.com about any payment problem.
- Can I share my results with my doctor?
- Yes. You receive the report as a PDF and can show it to your doctor. The introduction explains what each column and score means.
- Can I check that nothing is uploaded?
- Yes. Open your browser's developer tools (Network tab) while a report generates: no request carries your DNA file or the PDF. The file is parsed in memory by a WebAssembly module and the PDF is written on your device.
- Who is behind Full Human Health?
- Full Human, an independent software maker whose terms are governed by Swiss law, co-founded by Floriel Fedry (author of PurgeCSS, creator of Orphos) and Michèle Pfister. There is no data business: we hold no DNA to sell or share.
- Does it include ancestry or appearance traits?
- No. The reports cover health conditions in 17 sections and nutrition-related traits. There is no ancestry, relative matching or appearance report.
- Is this medical advice?
- No. Reports are informational and link to the underlying studies. Share the PDF with your doctor before making health decisions.
08 — Ready when you are
One $5.00 PDF, generated on this device.
Create an account, buy one credit, open your raw file. Nothing is uploaded, and a failed generation is refunded automatically.