GenoSight.ai turns raw
DNA data
into readable
health reports.
Upload a raw DNA file from 23andMe, AncestryDNA, or MyHeritage. GenoSight matches supported variants to curated evidence and explains the findings in plain language.
TXT, CSV, or TSV. Free to start. Your raw file is not sent to the AI model.
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Topical reports across nutrition, sleep, fitness, more
Curated variants from 16 evidence sources
PharmGKB evidence levels for medication-response context
From upload to your first findings
Don't have your data yet?
Get your raw file from a supported provider
Tap a provider for the fastest download path.
Why GenoSight
More context from the raw DNA file you already have.
GenoSight checks supported variants against curated evidence, explains the findings in plain language, and shows what your file does not cover.
More context from your existing DNA file.
Use a compatible 23andMe, AncestryDNA, or MyHeritage genotype file to explore supported variants beyond the summary supplied by your testing provider.
Reports shaped by your genotype and goals.
GenoSight combines supported variants with the optional health profile you provide, then shows the evidence level and limits for each finding.
Medication-response context.
Supported variants in genes such as CYP2C9, CYP2C19, SLCO1B1, and DPYD are shown with stronger PharmGKB evidence and a reminder to discuss medical decisions with a clinician.
Ask follow-up questions.
Once your report is ready, ask about its findings in plain language. Answers stay grounded in the report context and point back to the available evidence.
Features
Everything in your report.
Explore supported findings, their evidence, and follow-up questions in one report workspace.
21 topical reports across nutrition, fitness, sleep, and more
Metabolism
Neuro
Performance
Longevity
Findings by category
How it works
From raw data to insights in minutes.
Upload your DNA file
Drag in your raw data from 23andMe, AncestryDNA, or MyHeritage. We validate the file and store it privately with encryption at rest.
Build your health profile
AI-guided chat captures your symptoms, supplements, family history, and goals. Everything is optional and skippable.
Generate your report
GenoSight checks supported variants against curated evidence sources and includes only the report sections your file can support.
Chat with your findings
Ask follow-up questions, review population context, and prepare questions for a clinician, all grounded in your report findings.
Features
What you'll discover.
Supported findings, evidence levels, and clear coverage limits.
Lifestyle Variant Context
Drug metabolism, methylation, neurotransmitters, caffeine, sleep, fitness, nutrition, and 9 more categories with impact scoring.
ClinVar Variant Scan
ClinVar-sourced variant context with confidence stars and clinical-confirmation reminders.
Drug-Gene Interactions
PharmGKB Level 1A-2B evidence to support medication discussions with a clinician.
AI Chat Follow-Up
Ask questions about your results and get explanations grounded in your report findings.
Why does coffee keep me up so long? My CYP1A2 says slow.
Slow CYP1A2 metabolizers clear caffeine 2-3x more slowly than fast ones, so an afternoon coffee can stay active well into the evening. Many slow metabolizers find an early-afternoon cut-off improves sleep.
GWAS Catalog evidence | Educational, not medical advice
PDF Report Delivered
Download a PDF copy of your report for your records or a conversation with a clinician.
Private Storage Controls
Genome files are stored privately, protected in transit, and governed by row-level access controls.
Preview
See what your report looks like.
A comprehensive, AI-synthesized analysis of your genetic data.
Open full sample reportExample layout | ~600,000 SNPs typical for a consumer-chip upload
Executive Summary
Analysis of your genome identified 47 lifestyle findings across 16 categories, 12 medication-response findings with PharmGKB evidence, and 3 variants marked for clinician or genetic counselor discussion. Priority findings include CYP2D6 metabolizer context, MTHFR C677T heterozygous, and APOE e3/e4.
Priority Findings
Simple credit-based access.
Reports cost 100-350 credits by depth. Findings chat costs 1 credit per message.
Free trial
For trying your first reports
Usually enough for one deeper report or two lighter reports.
250 signup credits
No card required.
- Try GenoSight before paying
- 1-2 reports from anywhere in the library
- Onboarding chat free; findings chat costs credits
- Upgrade when you need more credits
- No card required, upgrade whenever
Monthly
For active exploration
Unlock roughly one third of the report library, plus plenty of chat.
1,500 credits every month
Sign in first, then Stripe checkout.
- Active monthly exploration
- About one-third of the report library each month
- Findings chat at 1 credit per message
- Top up with credit packs anytime
- Cancel anytime
Yearly
For full-library use
Billed $99.99 annually
Enough for every current report, regenerations, and long-term chat.
18,000 credits every year
Sign in first, then Stripe checkout.
- Best value for ongoing planning
- Covers the full 21-report library
- Generous buffer for follow-up chat
- Top up with credit packs anytime
- One renewal per year, cancel anytime
Lifetime
For long-term access
The full library every month, for life. Covers heavy real-world use.
6,000 credits every month, for life
Sign in first, then Stripe checkout.
- Lifetime access: pay once, keep forever
- Full library, every month, forever
- Generous chat under fair-use cap
- Top up with credit packs (rarely needed)
- One-time payment, no renewals ever
FAQ
Frequently asked questions.
Everything you need to know before getting started.
Which DNA testing services are supported?
GenoSight supports raw genotype files from 23andMe versions 3, 4, and 5, AncestryDNA, and MyHeritage. Upload the text-based genotype file from your provider, not a customer-facing PDF.
How do I get my raw DNA data file?
Each supported provider includes a raw-data download in its account settings. The GenoSight guide has step-by-step download instructions for 23andMe, AncestryDNA, and MyHeritage.
How do credits work?
Topical reports cost 100 to 350 credits depending on depth, findings chat costs 1 credit per message, and onboarding chat is free. New accounts receive 250 credits with no card required.
How is my genetic data protected?
Raw files are stored privately with encryption at rest. Row-level database security and server checks restrict access to your account, and raw genotype files are not sent to the AI model.
How accurate are the results?
GenoSight reports educational evidence, not a diagnosis. Disease-variant context uses ClinVar confidence levels, medication-response context is limited to stronger PharmGKB evidence, and each finding shows its evidence level and limits.
How long does analysis take?
Most file analyses complete in under 60 seconds. Larger topical reports can take longer while the report is generated.
Is GenoSight a medical diagnostic tool?
No. GenoSight provides educational genetic information and does not replace clinical testing or a healthcare professional. Discuss findings that could affect medical care with a qualified clinician or genetic counselor.
Can I delete my data?
Yes. Account deletion schedules removal of your genome file, reports, chat history, and associated records. You can cancel deletion within 30 days; after that period the deletion runs automatically.
Can my doctor or genetic counselor use the report?
The downloadable PDF can be used as an educational discussion document with a clinician or genetic counselor. GenoSight is not a clinical decision-support tool, and important findings may need confirmation through clinical testing.
What if my DNA file does not cover a variant I'm interested in?
Consumer genotype files assay hundreds of thousands of positions, so untyped variants are expected. GenoSight shows which supported variants were found and which report sections your file can support.
See what your raw DNA file contains.
Upload a compatible file and start with an educational report. No credit card is required.
250 free credits on signup. No credit card required. Educational insights, not a medical diagnostic.