DNA analysis from your 23andMe, AncestryDNA or MyHeritage raw file
Upload your raw DNA file and we explain, in plain language, what the matches found in it mean — and what they do not. Your file is processed and discarded, it is never sold, and you can delete the analysis whenever you like.
Coverage & actionable findings free · Full report 10 € · Private
What your raw data doesn't tell you
Your DNA file is just letters until someone reads it against the research.
# rsid chromosome position genotype rs4988235 2 136608646 AG rs1801133 1 11856378 -- rs6025 1 169519049 CT rs429358 19 45411941 CT rs7903146 10 114758349 CT … 600,000 more lines
Your raw DNA file
Around 600,000 lines of rsIDs and A/C/G/T. Technically your genome — practically unreadable.
Want to see what the file looks like inside? An annotated example of the four columns →
Your genotype at this variant, the trait the study measured, and a link to the source — not an overall risk score.
Illustrative example · synthetic data
Your report
The same data cross-referenced against open catalogues (GWAS, PharmGKB, ClinVar): matching variants, drug annotations and plain-language explanations.
How it works
From raw DNA file to personalised report in three steps.
Download your raw DNA
Get your raw data file from 23andMe, AncestryDNA, or MyHeritage. It's free and takes a few minutes.
Step-by-step guide →Drop your raw DNA file here
.txt, .csv or .zip · max. 50 MB
Upload to dnainfolab.org
Drop your file. It is encrypted in transit through our network (Cloudflare), processed and discarded, and your data is never sold or handed on.
Get your personalised report
See the variants your file contains per category, pharmacogenomics, and AI-powered explanations.
To see your own results, upload your raw DNA file and generate a private report.
What you'll get
This is what a report looks like: your variants, drugs, AI explanations and SNP search in one place.
Variants found
- Type 2 Diabetes
- 187 variants analysed
- Cardiovascular Health
- 96 variants analysed
- Alzheimer's Risk
- 214 variants analysed
- BMI & Obesity Predisposition
- 58 variants analysed
Illustrative example · synthetic data
Your variants, by research area
10 research areas: every matching variant in your file, the trait each study measured, and a link to it.
Pharmacogenomics
How your genetics may affect your response to drugs (warfarin, metformin, SSRIs…), with each annotation’s evidence level.
AI-powered explanations
Plain-language text grounded in PubMed, per category and in your language.
SNP search
Any rsID: your genotype, its population frequency and the traits associated with it.
Your DNA, your data
Your file is encrypted in transit, processed and discarded. We keep only the extracted variants and your results in the EU. A network and security provider is involved during upload and, only if you request an explanation, an external AI provider processes the necessary results —never the file—. We do not sell your data or use it for advertising. You can delete the analysis whenever you like.
See the providers and international transfers in our Privacy Policy →Built on open, peer-reviewed science
Calibration & limits
We are clear about what these numbers can and cannot tell you. How much of each area your file covers varies — and that is information too.
Chip coverage
Each category reports how many of the variants we track your file actually contains. It reports no overall score — see the methodology for why we withdrew it.
variants shown per categoryAncestry bias
The research was done mostly in people of European ancestry. For other ancestries, the effects it reports may not transfer.
flagged in the reportNot a diagnosis
Information grounded in published science — not medical advice, and not an individual prediction.
informational onlyScientific content last reviewed:
Genuinely free · 10 € for the full report
Actionable findings without paying. The full report, once.
Free, whether or not you buy
€0
Always included
- Which research areas your DNA matched, and how much of each one your file covers
- Records meeting this report's clinical and review criteria (ClinVar, 2+ review stars)
- Drug interactions with strong evidence (PharmGKB 1A/1B)
These are shown whether or not you buy the report. A well-reviewed variant or a documented drug interaction is not something to hold back.
Upload your DNA freeMy DNA explained
€10.00
One payment, taxes included. No subscription, no later charges.
- The plain-language explanation of every match found in your DNA, across the 10 research areas
- What each result means and, above all, what it does not mean
- An ordered report you can move through: area by area, finding by finding
- The complete ClinVar section, with context and sources for every finding
- The complete pharmacogenetics section, drug by drug
- Scientific mode: the published figure behind each finding, with its unit and its studies
- SNP search: look up any variant in your own file
- PDF export, full and clinical
- A read-only link to share the report with whoever you choose
- Access for as long as your account stays active
If you do not buy the report, the analysis is deleted automatically after 30 days: we do not keep the genetic data of people who did not buy.
Frequently asked questions
Is this a medical diagnosis?
No. This is a research-based informational tool using published GWAS studies. It's not a diagnosis and should never replace advice from a qualified healthcare professional.
How accurate are the results?
The report predicts nothing, so there is no accuracy figure to quote. What it gives you is which studied variants are in your file, the trait each study measured and the effect it published. Two things bound that: how many of the relevant variants your file contains, which we show for every area, and the population bias of the underlying studies, mostly European ancestry. That figure is coverage — how much of the research your file can be checked against. It is not a confidence level and not a measure of how much to trust a finding.
Can I delete my data?
Yes. Any uploaded analysis can be deleted from the history page. You can also delete your entire account from settings — this removes all SNPs, scores, and personal data permanently.
Do you share my DNA with anyone?
No. Your data is used only to generate your report. We don't share, sell, or license it to research institutions, insurers, or any third party.
Which DNA providers are supported?
23andMe (.txt), AncestryDNA (.txt), and MyHeritage (.csv). You need the raw DNA data file — not the health/ancestry PDF reports.
Is it free?
Part of it genuinely is, and part of it is paid. Free whether you buy or not: the clinically-reviewed ClinVar variants that affect you (2 or more review stars) and the strong-evidence drug interactions (PharmGKB 1A and 1B) — we do not withhold an actionable finding behind a payment. The full report costs 10,00 € once per report, taxes included, and what it gives you is the explanation of what the matches found in your DNA mean; everything it includes is listed on the pricing card on this page. If you do not buy it, the analysis is automatically deleted 30 days after you upload it.
What if I'm not of European ancestry?
Be cautious with the numbers. The GWAS studies behind these associations have historically over-represented people of European descent, so an effect measured there may be different, or absent, in African, East Asian, South Asian, Hispanic/Latino and other ancestries. The platform surfaces this on every report with a prominent banner. The underlying rsID associations are still informative, and the effect sizes they report were measured in a population that may not match yours. Use the results as a starting point for conversation with a clinician, not as a definitive answer.
From our blog
Honest explainers about the science behind your DNA.
23andMe Raw Data File Explained
The four columns, the genome build, no-calls and file size — what your 23andMe raw file actually contains, in plain English.
Read →23andMe Raw Data Analysis: What You Can and Cannot Learn
The honest scope of a raw data analysis — research associations, drug response and traits you can learn, and the hard limits you cannot cross.
Read →How to Interpret Your 23andMe Raw Data: A Practical Guide
A practical guide to reading and analysing the raw DNA file from 23andMe — what it contains, three ways to interpret it, and the limits to keep in mind.
Read →Ready to explore your DNA?
Coverage and actionable findings free. Full report 10 € once. Your data stays private.