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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 PDF with a section for every category that has a condition for you: 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
- 409
- catalog traits, 17 categories
- 1,020
- 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 tendency, the evidence, and the study behind it.
01
A tendency per condition
Higher odds, lower odds or no meaningful difference, from your copies of the risk alleles at every compared variant, set against the average person's. When your file measures fewer than a third of the variants known for a condition, or fewer than a third of those known variants can be compared, the report says so instead of guessing.
02
The evidence table
rsID · your genotype · risk allele · copies · frequency · effect per copy · PubMed IDs. One row per variant at which you carry the risk allele, so you or your doctor can check each one against its study.
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 one lead variant per region, without modeling finer linkage between variants. How the tendency 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
Two reports: your health and your nutrition.
Every category, one PDF
Complete health report
Every category with a condition for you in one PDF (14 to 16 sections): risk alleles, your genotype, effect size (odds ratio) 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.
What the health report covers
The complete health report contains every category with a condition for you (14 to 16 sections). Categories are not sold as separate reports: on its own, a category can hold too few conditions your file measures to tell you much.
- 01Autoimmune & inflammatory
- 02Cancer
- 03Cardiovascular
- 04Congenital
- 05Dental & oral health
- 06Dermatological
- 07Endocrine & metabolic
- 08Gastrointestinal
- 09Infectious diseases
- 10Musculoskeletal
- 11Neurological & mental health
- 12Obstetrics & gynecology
- 13Other conditions
- 14Reproductive
- 15Respiratory
- 16Urological
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 can also be used for an adult family member's file, with their explicit consent.
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 · 14 min read
How to Read a DNA Health Report: SNPs, Genotypes, Risk Alleles, Odds Ratios and the Tendency
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 tendency per condition compares your copies of each risk allele with the average person's, weighted by the study's effect; it keeps one lead variant per region but does not model finer linkage between variants, and it is not a clinical polygenic risk score. Treat 'higher odds' as a prompt to talk to a doctor, not as a diagnosis.
- What do higher odds, lower odds and no meaningful difference mean?
- They compare the risk-allele copies you carry with the copies the average person carries, variant by variant. Your copies above or below average at each variant, times its log odds ratio, are added up, and the sum, taken back to an odds ratio, is your odds relative to the average person. 'Higher odds' means 1.20 or more, 'lower odds' 0.83 or less, and 'no meaningful difference' means between 0.83 and 1.20 (for measured levels in the nutrition report: within ±0.20 standard deviations, or within ±2.0 net copies when only the direction of each effect can be counted). 'Not assessable' means your file measures fewer than a third of the variants known for that condition; 'not comparable' means fewer than a third of those known variants could be compared with the average person.
- Which conditions are covered?
- Up to about 190 conditions, grouped by category into 14 to 16 sections of one complete health report, from coronary artery disease and atrial fibrillation to celiac disease, psoriasis and rheumatoid arthritis, plus a separate nutrition report. The sample report shows how the health 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, for adults who agree. Credits are not tied to a file: pick a raw file for each report. An adult partner, parent, child or sibling can get their own PDF from your account once they have explicitly agreed to the analysis, and nothing is uploaded for any of them. Do not analyze the file of a minor, or of anyone who has not agreed or cannot agree.
- 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. A credit used for a generated report cannot be refunded. If you are a consumer in the EEA or the UK, you can withdraw from a purchase within 14 days for the credits you have not used yet: write to support@full-human.com, which is also the address for 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 each tendency 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. There are two reports: a complete health report, with conditions grouped by category, and a nutrition report. There is no ancestry, relative matching or appearance report.
- Is this medical advice?
- No. Reports are informational: they are not a diagnosis or a medical genetic test, and they 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.