Decode your DNA.
Unlock your potential.
Transform raw genetic data from 23andMe, AncestryDNA, and MyHeritage into readable educational health reports. Powered by AI.
Attach your raw DNA data to start for free, no credit card required
Already know you want deeper reports? Choose monthly
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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
Most of what your DNA says,
you have never seen.
Three analysis engines run against your raw genotype file. Findings are graded by evidence level, written in plain language, and stored only for you.
Your raw data is sitting unread.
23andMe and AncestryDNA hand back a download link and call it done. Your file holds 600,000+ SNPs, almost none surfaced in the customer report.
Generic reports don't reflect you.
Off-the-shelf wellness apps run the same handful of SNPs for everyone. We curate 16,000+ variants across 16 evidence sources and score them against your specific genotype, your symptoms, and your stack.
Pharmacogenes are in your DNA.
CYP2C9, CYP2C19, SLCO1B1, DPYD: variants in these metabolism genes are graded by PharmGKB and used by clinicians worldwide. We surface yours so a future medication conversation starts with context, not guesswork.
Static PDFs answer the wrong questions.
Once your report is ready, ask follow-ups in plain language. Claude grounds every answer in your findings, with citations to the underlying evidence level.
Features
Everything in your report.
Three analysis engines and an AI chat interface, built around the evidence layer most consumer reports leave out.
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 parse it locally and store it encrypted.
Build your health profile
AI-guided chat captures your symptoms, supplements, family history, and goals. Everything is optional and skippable.
Generate your report
Eight engines cross-reference 16,000+ curated variants with your profile. The report self-omits sections without data.
Chat with your findings
Ask follow-up questions, compare to populations, propose stack changes, all grounded in your specific results.
Features
What you'll discover.
Three analysis engines. One comprehensive report.
79 Lifestyle SNPs Analyzed
Drug metabolism, methylation, neurotransmitters, caffeine, sleep, fitness, nutrition, and 9 more categories with impact scoring.
341K Disease Variants Scanned
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. Get personalized explanations powered by Claude AI.
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
Professional-grade report emailed to you and available for download anytime.
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.
Ready to decode your DNA?
Upload your file and get personalized insights in under 60 seconds. Free tier available, no credit card required.
250 free credits on signup. No credit card required. Educational insights, not a medical diagnostic.