Your DNA. Your Health. Your Control.
Upload your genome file. Get personalized guidance for better sleep, smarter nutrition, the right supplements, optimized workouts, medication safety, and 21 health categories — all decoded from your DNA.
HIPAA-compliant · AES-256 encrypted · GINA-protected · how we protect your data
From Upload to Insight
Upload your raw genome file from any provider — or any standard VCF file. Auto-detected instantly.
Our pipeline analyzes your DNA across 21 health categories, cross-referencing millions of clinical studies to find what matters for your body.
Get clear, actionable recommendations for supplements, nutrition, sleep, fitness, and more — all personalized to your genetics.
And it doesn't stop there — your dashboard updates as new variants are discovered, and Helix is on call whenever you have a question.
Full Transparency
No black box. See the clinical evidence behind every finding, and exactly what we're measuring.
Open Variant RegistryBacked by 2.97M clinical annotations from ClinVar, GWAS Catalog, and PharmGKB, plus 77.5M REVEL pathogenicity scores.
Before & After
One-size-fits-all health advice was never built for you. Here's what changes when your health is guided by your actual genetics.
Taking random supplements from a blog post
A supplement plan built from YOUR variants — with exact dosages and priority scores
Following a generic diet that never seems to work
Eating for YOUR metabolism — caffeine, dairy, folate, gluten, all decoded
Forcing a morning routine that fights your biology
A sleep strategy matched to your circadian genetics
Taking random supplements from a blog post
A supplement plan built from YOUR variants — with exact dosages and priority scores
Following a generic diet that never seems to work
Eating for YOUR metabolism — caffeine, dairy, folate, gluten, all decoded
Forcing a morning routine that fights your biology
A sleep strategy matched to your circadian genetics
Training based on what worked for someone else
Workouts matched to your muscle fiber type and recovery speed
Taking medications without knowing if they work for you
200+ drug interactions checked — know before you fill the prescription
Getting a DNA report once and never looking at it again
A living dashboard that updates as new variants are discovered and research evolves
21 Categories
Not just one thing. Everything — from how you sleep to what you eat to which medications actually work for you. Organized by what matters to your daily life.
Energy, sleep, mood, and immunity
What your body actually needs — not generic advice
Your natural rhythm and optimal sleep strategy
Cognitive traits, focus, and mental wellness
How you burn fuel and why you crash at 2pm
Immune strength, inflammation, and autoimmune risk
Thyroid, cortisol, and hormone balance
Energy, sleep, mood, and immunity
What your body actually needs — not generic advice
Your natural rhythm and optimal sleep strategy
Cognitive traits, focus, and mental wellness
How you burn fuel and why you crash at 2pm
Immune strength, inflammation, and autoimmune risk
Thyroid, cortisol, and hormone balance
Skin, aging, and appearance
Elasticity, sun sensitivity, and conditions
Cavity risk, gum health, and enamel strength
Biological aging markers and longevity genes
Fitness, strength, and recovery
Power vs endurance, recovery speed, injury risk
Bone density, joint health, and connective tissue
Digestion, food sensitivities, and microbiome
Prevention, medications, and screening
200+ drug interactions — know before you fill
Heart disease risk and cholesterol metabolism
Cancer risk genes and screening guidance
Fertility, carrier status, and family planning
Predispositions and sensitivities
Genetic factors in vision and hearing
Screening for rare genetic conditions
Kidney function and renal health
+ Full ancestry & heritage composition included with every upload
Enterprise-Grade Security
Genomic data is the most personal data you have. We treat it that way.
Already Tested?
If you've ever done a DNA test, you have a raw data file sitting unused. Upload it to Atlagene and unlock 21 health categories your original provider never analyzed.
23andMe, AncestryDNA, MyHeritage, and similar. Export your raw data file and upload — takes 2 minutes.
Any standard VCF file from a lab, research study, or clinical test. Auto-detected and analyzed.
Nebula, Dante Labs, or clinical WGS files get the deepest analysis with 7x more variants. Requires Premium.
Simple Pricing
No hidden fees. Upload your data for free and see real results before you pay anything.
Comprehensive genomic health for your entire family. Includes unlimited physician reviews for all members, parent-child genetic matching, and per-member analysis. Starts at $39.99/mo or $349/year (save 27%) for 2 members — add more for $9.99/mo each.
Questions
We accept raw data files from 23andMe, AncestryDNA, MyHeritage, and similar consumer tests, as well as any standard VCF file from clinical labs or research studies. Files are auto-detected on upload.
Consumer array files (23andMe, AncestryDNA) are analyzed in under 2 minutes. Whole genome sequencing (WGS) files take 3–5 minutes due to their larger size.
Yes. You can cancel your Premium or Family subscription at any time from your account settings. Your data and free-tier access remain available after cancellation.
Your genome data stays encrypted in our HIPAA-compliant infrastructure. You retain free-tier access to your results. You can request full data deletion at any time.
Your genome is stored in AES-256 encrypted, isolated databases. We are HIPAA and GINA compliant, and your genetic data is never sold or shared with third parties.
No — if you’ve already done a 23andMe, AncestryDNA, MyHeritage, or any other DNA test, just export your raw data file and upload it. Atlagene works with what you already have. (Atlagene-branded collection kits will be available in a later release.)
Upload your genome for free. Get personalized guidance for sleep, nutrition, supplements, fitness, medications, and more — all from your DNA.
Upload Free — Get Started