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Your DNA. Your Health. Your Control.

Your DNA Is the Manual
You Were Never Given

Turn any genome into a complete genetic health analysis across 21 health categories. One pipeline, two ways in — for individuals who want to understand their own DNA, and for diagnostic labs that need genomic analysis infrastructure without the bioinformatics team.

Upload Free — Get StartedFor labs & clinics
Built on 2.97M clinical annotationsGeneticist-curated variant registryHIPAA-grade · BAA available

AES-256 encrypted · Never sold or shared · how we protect your data

21
Health Categories
45964
Genetic Markers Analyzed
2.97M
Clinical References
24/7
Helix AI Chat

One Pipeline, Two Ways In

Built for Labs and Individuals

The same 21-category analysis engine, packaged for the way you work — whether you run a diagnostics lab or just have a DNA file of your own.

For Diagnostic & Clinical Labs

Genomic analysis infrastructure

Pay-per-test 21-category analysis with white-label branded reports. No bioinformatics team to hire, no subscription, no minimums.

  • Full 21-category pipeline per test
  • Branded PDF reports for your patients
  • $49 → $25/test volume pricing
  • BAA available · API access
For Labs
For Individuals

Own your DNA

Upload a genome file you already have and unlock personalized guidance across 21 health categories, with Helix AI on call to explain it all.

  • 21 health categories from your DNA
  • Helix AI explains every finding
  • All results shown — no hidden data
  • Free to start, no kit required
Upload Free

For Labs

Genomic analysis infrastructure, pay-per-test

The same pipeline that powers our consumer platform — repackaged for clinical workflows. Upload patient genomes, get branded reports back.

21-category pipeline

Cardiovascular, oncology, pharmacogenomics, and 18 more — every test gets the complete panel.

White-label branded reports

Clinical PDF reports carrying your lab’s logo, or Atlagene branding. Your choice, per test.

$49 → $25/test, no subscription

Pay only for what you run. Volume discounts kick in automatically. No setup fees, no minimums.

BAA + API

HIPAA-grade · BAA available. Batch upload via API, isolated PII/genomic architecture.

White-label clinical genomic report on a tablet with a risk gauge and charts
Lab analytics dashboard showing test volume, throughput, and per-test billing
Talk to SalesExplore the Lab Portal
Clinician showing a patient their genomic report on a tablet

The Flywheel

Your lab does the acquiring

The lab portal is a zero-CAC patient-acquisition channel. Every test you run is a warm introduction to a future longitudinal member.

  1. 1

    Your lab runs the test

    Upload a patient genome, get the 21-category analysis + branded report back. Pay per test.

  2. 2

    Patient handoff

    With patient consent, invite them to an Atlagene consumer account from their report.

  3. 3

    They become a member

    You keep the relationship; Atlagene handles the longitudinal experience. ~5–10% convert.

5–10% expected patient conversion

From Upload to Insight

How It Works

1

Upload Your Data

Upload your raw genome file from any provider — or any standard VCF file. Auto-detected instantly.

2

AI-Powered Analysis

Our pipeline analyzes your DNA across 21 health categories, cross-referencing millions of clinical studies to find what matters for your body.

3

Personalized Guidance

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

Browse Every Variant We Analyze

No black box. See the clinical evidence behind every finding, and exactly what we're measuring.

Open Variant Registry

Backed by 2.97M clinical annotations from ClinVar, GWAS Catalog, and PharmGKB, plus 77.5M REVEL pathogenicity scores.

Before & After

Generic Advice vs. Your DNA

Generic health advice was never built for you. The owner's manual for the genetic blueprint you were given is finally readable — variant by variant. Here's what changes when your health is guided by your actual genetics.

Before

Taking random supplements from a blog post

With Atlagene

A supplement plan built from YOUR variants — with exact dosages and priority scores

Before

Following a generic diet that never seems to work

With Atlagene

Eating for YOUR metabolism — caffeine, dairy, folate, gluten, all decoded

Before

Forcing a morning routine that fights your biology

With Atlagene

A sleep strategy matched to your circadian genetics

21 Categories

Your Complete Health Map

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.

Feel Better

Energy, sleep, mood, and immunity

Nutrition & Diet

What your body actually needs — not generic advice

Sleep & Circadian

Your natural rhythm and optimal sleep strategy

Brain & Mood

Cognitive traits, focus, and mental wellness

Energy & Metabolism

How you burn fuel and why you crash at 2pm

Immunity

Immune strength, inflammation, and autoimmune risk

Hormonal & Endocrine

Thyroid, cortisol, and hormone balance

+ Full ancestry & heritage composition included with every upload

Enterprise-Grade Security

Your Data, Protected

Genomic data is the most personal data you have. We treat it that way.

HIPAA-Grade Security
AES-256 Encryption
Geneticist-Curated
Isolated Architecture
GINA Protected
Audit-Ready Architecture

For diagnostic & clinical labs

BAA availableAPI accessIsolated PII / genomic architectureAudit-ready

Already Tested?

Got a Genome File? You're Already Halfway There.

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.

Consumer DNA Tests

23andMe, AncestryDNA, MyHeritage, and similar. Export your raw data file and upload — takes 2 minutes.

Clinical & Research Files

Any standard VCF file from a lab, research study, or clinical test. Auto-detected and analyzed.

WGS / Whole Genome

Nebula, Dante Labs, or clinical WGS files get the deepest analysis with 7x more variants.

23andMe raw data file format compatibleAncestryDNA raw data file format compatibleNebula Genomics raw data file format compatibleDante Labs raw data file format compatible

23andMe, AncestryDNA, Nebula Genomics, and Dante Labs are trademarks of their respective owners. Atlagene is not affiliated with these companies; logos shown for file-format compatibility reference.

Simple Pricing

Pricing for Individuals & Labs

No hidden fees. Individuals upload for free and see real results before paying; labs pay per test, with no subscription.

For Individuals

Free
$0
forever
  • 5 health categories included
  • All results shown (no hidden data)
  • Basic Helix chat (3 msg/day)
  • Physician review from $35/result
Get Started Free
Most Popular
Premium
$14.99/month
or $119/year (save 34%)
  • All 21 health categories
  • Pharmacogenomics (200+ drugs)
  • Unlimited Helix AI chat
  • Personalized supplement plan
  • Polygenic Risk Scores
  • Health alerts + reminders
Start Premium
Premium + Physician
$29.99/month
or $249/year (save 31%)
  • Everything in Premium
  • Unlimited physician reviews bundled
  • 1 consultation per quarter included
  • Pharmacogenomics medication report
  • Priority physician review (<48h)
Start Premium +
Family PlanNEW

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.

Start Family Plan
Compare all plans & annual pricing

For Labs · Pay Per Test

No subscription, no minimums. The same 21-category pipeline; volume discounts apply automatically.

Standard
$49/test
No minimums. Pay only for what you run.
  • Full 21-category analysis
  • Atlagene-branded PDF report
  • Standard turnaround (<5 min)
  • OTP email login
Talk to Sales
Most Common
Volume
$35/test
51–200 tests per month
  • Everything in Standard
  • White-label PDF (+$10/test)
  • API access for batch upload
  • Priority queue (+$15/test)
Talk to Sales
Enterprise
$25/test
200+ tests per month
  • Everything in Volume
  • Dedicated account manager
  • Custom report templates
  • BAA + DPA on request
Talk to Sales
See the full Lab Portal

Questions

Frequently Asked

What file formats do you support?

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.

How long does the analysis take?

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.

Can I cancel anytime?

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.

What happens to my data if I cancel?

Your genome data stays encrypted in our HIPAA-grade infrastructure. You retain free-tier access to your results. You can request deletion of your account and data at any time, processed per our privacy policy.

Is my genetic data safe?

Your genome is stored in AES-256 encrypted, isolated databases. We follow HIPAA-grade security practices, and your genetic data is protected under GINA, and your genetic data is never sold; it is shared only with the service providers that operate Atlagene, under contractual confidentiality, or with a physician you ask to review it.

Do I need to take a new DNA test?

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.)

For labs: is a BAA available?

Yes. Atlagene runs on HIPAA-grade infrastructure and a Business Associate Agreement (BAA) is available for lab and clinical partners, alongside a DPA on request.

For labs: what’s the turnaround at volume, and is there API / white-label access?

Consumer arrays return in under 2 minutes and WGS files in 3–5 minutes, with a priority queue available. Volume tiers add API access for batch upload and white-label PDF reports carrying your lab logo.

For labs: who owns the patient data we send?

The lab and its patients own the data. We process it only to return your analysis and reports — patient data is never used to build a competing product, and genomic data is stored isolated from PII.

Stay In The Loop

Genomic Health, Monthly. No Fluff.

New variant explainers, pharmacogenomics deep-dives, platform updates. Unsubscribe anytime.

Your Body Has Answers. Start Reading.

Upload your genome for free. Get personalized guidance for sleep, nutrition, supplements, fitness, medications, and more — all from your DNA.

Upload Free — Get StartedTalk to Sales