23andMe
Tab-separated raw genotype exports.
Aquest contingut encara no està disponible en català. El mostrem en anglès.
For raw DNA files you already own
Analyse your raw DNA data
Turn a file of rsIDs and genotypes into a structured report that separates clinical records, medication evidence and research associations — with the limitations beside the findings.
- ✓ No subscription
- ✓ Processed on EU infrastructure
- ✓ Your original file is discarded after parsing
Free results firstSynthetic preview
A report with three evidence zones
ClinVar records
Matches to imported ClinVar variants, with classification, review status, related conditions and source identifiers.
Pharmacogenomics
PharmGKB annotations that match the genotype in your file, shown with evidence level and source context.
Research associations
GWAS associations across the report’s research areas, with the measured trait, published effect and study provenance.
Compatible raw DNA providers
DNA Info Lab accepts the exported text, CSV or ZIP formats its parser can recognise. Compatibility means we can read the file; it does not mean every chip tests every relevant position.
What the analysis can show today
Your genotypes are matched against three distinct evidence sources. They stay separate because a clinical record, a drug annotation and a research association do not answer the same question.
ClinVar records
Matches to imported ClinVar variants, with classification, review status, related conditions and source identifiers.
Pharmacogenomics
PharmGKB annotations that match the genotype in your file, shown with evidence level and source context.
Research associations
GWAS associations across the report’s research areas, with the measured trait, published effect and study provenance.
See useful findings before deciding
Uploading and processing the file is free. The free view shows coverage and the defined actionable findings; the paid report unlocks the complete interpretation and tools.
Free analysis
€0
- ✓Coverage across the research areas, including areas with no matches.
- ✓Counts kept in their real units: areas, physical ClinVar variants and unique medicines.
- ✓High-confidence ClinVar and PharmGKB 1A/1B findings defined by the product contract.
El meu ADN explicat
€10.00
Pagament únic, impostos inclosos. Sense subscripció ni càrrecs posteriors.
- L'explicació en llenguatge clar de cada coincidència trobada al teu ADN, a les 10 àrees de recerca
- Què significa cada resultat i, sobretot, què no significa
- Exportació a PDF, complet i clínic
Veure tot el que inclou
- L'explicació en llenguatge clar de cada coincidència trobada al teu ADN, a les 10 àrees de recerca
- Què significa cada resultat i, sobretot, què no significa
- Un informe ordenat i navegable: àrea per àrea, troballa per troballa
- La secció ClinVar completa, amb context i fonts a cada troballa
- La secció de farmacogenètica completa, medicament per medicament
- Mode Científic: la xifra publicada de cada troballa, amb la seva unitat i els seus estudis
- Cercador de SNP: consulta qualsevol variant del teu propi fitxer
- Exportació a PDF, complet i clínic
- Un enllaç de només lectura per compartir l'informe amb qui tu decideixis
- Accés mentre el teu compte continuï actiu
Inspect the product before uploading
The public example uses synthetic genotypes and the same report components as a real analysis. It shows the simple and scientific reading modes, sources and premium boundary without exposing anyone’s DNA.
From raw file to report
- 1
Choose your export
Use the original raw DNA download from a supported provider; ZIP files are accepted when they contain a recognised export.
- 2
We parse and match it
The server detects the format, validates each row and compares usable genotypes with the current imported catalogues.
- 3
Read free results first
Your report is created before any checkout. You choose whether the complete report is worth the one-time price.
What happens to your DNA data
The original upload is parsed in memory and discarded. Extracted variants and derived report results are stored on the service’s EU infrastructure so you can return to the analysis, until you delete them or the applicable retention rule removes an unpaid analysis.
- ✓Raw genetic data is not sold and is not sent to advertising analytics.
- ✓Optional AI explanations send only the report context needed for that explanation, after you request it.
- ✓You can export or delete your account data from the product.
What this report cannot tell you
- It is not a medical diagnosis, clinical test or treatment recommendation.
- Consumer chips sample selected positions; an absent match does not prove an absent variant or risk.
- Research associations describe populations and published effects, not an individual outcome.
- Coverage and interpretation vary by provider, chip version, ancestry and catalogue evidence.
- Important health decisions require confirmation with an appropriate healthcare professional.
Coverage across 10 research areas
Sources and method, not a black box
The report identifies the imported dataset versions and links findings back to ClinVar, PharmGKB, the GWAS Catalog and cited publications. The methodology explains parsing, matching, effect direction, evidence filters, ancestry limits and what the product deliberately does not calculate.
Read the methodology →Raw DNA analysis questions
Is this a medical diagnosis?
No. It is an educational report based on selected positions in a consumer raw DNA file. Clinically important findings need professional confirmation.
Do I have to pay before seeing anything?
No. Uploading, processing, coverage and the defined free findings cost €0. The complete report is an optional one-time purchase.
Is the €10.00 payment a subscription?
No. It is one payment, taxes included, with no recurring subscription.
Does DNA Info Lab keep the uploaded file?
The original file is parsed in memory and discarded. Extracted variants and report results are stored until deletion or the stated retention limit.
Will every raw DNA file produce the same coverage?
No. Providers and chip versions test different positions, and catalogue coverage changes as scientific sources are updated.
Can I inspect a report first?
Yes. The public example is built from synthetic genotypes and requires no account or upload.
Ready to see what your raw DNA file contains?
Start free, review the findings your file actually supports and decide about the full report afterwards.
Start the free analysis →