For 23andMe & Ancestry users

Your DNA knows more than ancestry.

Upload your existing raw data for health risks, medication response, and 481 traits. Analyzed privately on your device.

Free to start Stays on device

$100 $49 once ยท 30-day money-back guarantee

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Health Risks

52 conditions

Cardiovascular, cancer, metabolic, and neurological risks, with odds ratios and percentile rankings against population data.

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Medication Check

101 drugs

See how your genes affect SSRIs, pain meds, statins, blood thinners, and more. Based on CPIC clinical guidelines.

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Genetic Traits

481 traits

Caffeine metabolism, sleep chronotype, pain sensitivity, muscle type, and hundreds more decoded from your DNA.

Example Findings from Real Reports

DPYD

5-FU Toxicity Risk

Chemo drug sensitivity flagged

Critical
CYP2D6

Poor SSRI Metabolizer

May need adjusted antidepressant dose

Actionable
SLCO1B1

Statin Myopathy Risk

Higher risk of muscle pain on statins

Discuss w/ Dr
APOE ฮต2

Alzheimer's Protection

40-50% reduced risk variant

Protective

See It In Action

Not Just Data. Personalized Insights

Most Detailed

Cognitive Profile

Your brain's genetic blueprint

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Learning Capacity

Room to optimize

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Working Memory

Room to optimize

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Processing Speed

Room to optimize

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Cognitive Resilience

Room to optimize

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Personalized Recommendation

Your BDNF variant is associated with enhanced response to aerobic exercise (30+ min, 4x/week), which research links to improved cognitive function.

Fan Favorite

Sleep & Circadian

Chronotype & sleep genetics

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Night Owl

CLOCK gene: CC genotype

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Sleep Depth

Deep Sleeper

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Sleep Talking

Higher risk

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Caffeine Sensitivity

Slow metabolizer

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Your Optimal Schedule

Based on your genes: Sleep 12:30amโ€“8:30am. Peak focus: 10amโ€“1pm & 4pmโ€“7pm.

Health Risks

52 conditions analyzed

Type 2 DiabetesElevated
Heart DiseaseModerate
Alzheimer'sAverage
52 conditions analyzed

These are just 3 of 27+ report tabs in your full analysis.

By the Numbers

Comprehensive Genetic Intelligence

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Research-Backed Variants Scanned

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Genetic Traits Decoded

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Report Tabs

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Private. Data Never Leaves Your Browser

Pricing

Simple, Transparent Pricing

Comparable services charge $99 to $199 every year. We charge once.

One-time payment. No subscription, no hidden fees

Free

Start with 30 traits instantly

$0
  • 30 genetic traits analyzed
  • Basic ancestry composition
  • Raw data browser
  • PDF export
  • Client-side processing

Premium

Unlock everything: 481 traits

$100$49one-time
Save 51% ยท launch pricing

30-day money-back guarantee ยท No questions asked

  • Everything in Free
  • All 481 genetic traits
  • Health risk analysis (52 conditions)
  • Pharmacogenomics (14 genes, 50+ drugs)
  • Cognitive & mental health profile
  • Sleep, athletic & longevity analysis
  • Action Plan & Risk Timeline
  • Lifetime updates
SelfDecode$99/year
Nebula$149/year
GenomeInsight$100$49 once

Launch pricing ยท One payment, lifetime updates ยท 30-day money-back guarantee.

Why GenomeInsight

What Makes GenomeInsight Different

๐Ÿ”’Privacy

100% Private

Your DNA file is processed entirely in your browser. Nothing is uploaded, stored, or shared. Ever. We literally can't see your data.

๐Ÿ’ฐPricing

One Payment, Not a Subscription

Pay $49 once and own your analysis forever. No monthly fees, no annual renewals, no surprise charges. SelfDecode charges $99 every year, over $297 across three years. Nebula charges $149/year.

๐Ÿ“ŠDepth

27 Reports, Not a Summary

Most DNA services give you a pie chart. We give you 27 interactive tabs: health risks with odds ratios, drug interactions, cognitive profile, sleep genetics, longevity score, and 481 decoded traits.

Our Sources

Powered by Real Research

Health risk and pharmacogenomics analysis drawn from leading clinical and genomics databases

ClinVar

NCBI clinical variant database

GWAS Catalog

Genome-wide association studies

PharmGKB

Pharmacogenomics knowledge base

CPIC

Clinical Pharmacogenetics Implementation Consortium

๐Ÿ”’ 100% In-Browser Analysis๐Ÿฅ GINA Protects You๐Ÿšซ Zero Data Storage๐Ÿ“‹ Peer-Reviewed Research

FAQ

Frequently Asked Questions

Everything you need to know about GenomeInsight.

Absolutely. GenomeInsight processes everything directly in your browser using client-side JavaScript. Your raw genetic data file is never uploaded to any server. No network requests are made with your DNA data. It stays on your device, period.

You can download your raw data from services like 23andMe, AncestryDNA, or MyHeritage. Each provider has a "Download Raw Data" option in their account settings. The file is typically a .txt or .csv file containing your genotyped SNP data.

Our analysis is based on peer-reviewed GWAS (Genome-Wide Association Studies), ClinVar pathogenicity classifications, CPIC pharmacogenomics guidelines, and established population genetics research. However, consumer genotyping covers only a fraction of your genome. Results are informational — not diagnostic.

No. GenomeInsight is strictly an educational and informational tool. It is NOT a medical device, diagnostic test, or clinical service. Genetic risk factors are just one piece of the puzzle — lifestyle, environment, and family history all matter. Always consult a qualified healthcare provider before making medical decisions.

We support raw data exports from 23andMe (.txt), AncestryDNA (.txt), MyHeritage (.csv), and standard VCF files (.vcf). The parser auto-detects the format and extracts SNP data accordingly.

No account is needed for the free tier. Simply visit the site, upload your file, and explore your traits and basic ancestry instantly. For health risks, pharmacogenomics, and premium reports, you'll create an account after purchasing.

Pharmacogenomics (PGx) studies how your genes affect your response to medications. For example, variants in CYP2D6 can make you a poor or ultra-rapid metabolizer of certain drugs like codeine or tamoxifen. Our report analyzes 14 pharmacogenes covering 50+ medications based on CPIC clinical guidelines.

Your genetic data is fixed, but our analysis database grows. As new research is published and we add more variants, re-uploading your file will give you an updated, more comprehensive report. Premium users get lifetime access to all future updates.

Upload your DNA, free30 traits free, no account needed