Public Benefit Corporation

What does your DNA reveal about you?

Everything — but only if you can read it.

ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA ACGT TGCA TT AC GG TC TT CCGTC AT GGC TAC GAT TTA CGC AGT TGG CAA TCG GTA
fast caffeine metabolismlactose intolerantalcohol flushneeds less sleependurance-builtrapid drug metabolizersalt-sensitiveanesthesia sensitivitycystic fibrosis carrieriron overload riskelevated clot riskhereditary cancer riskelevated alzheimer's riskfast caffeine metabolismlactose intolerantalcohol flushneeds less sleependurance-builtrapid drug metabolizersalt-sensitiveanesthesia sensitivitycystic fibrosis carrieriron overload riskelevated clot riskhereditary cancer riskelevated alzheimer's risk
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Your DNA affects every part of your life.

Genome Assistant

Private & encrypted

Finding the right medication is usually trial and error. Your DNA can shortcut it. Want to see?
Yes, show me

You're a CYP2C19 rapid metabolizer (only about 1 in 4 people are), so you clear several common medications, like some antidepressants and the blood thinner clopidogrel, faster than average. A standard dose can wear off before it fully works, so it's worth sharing with your prescriber to get the dose right the first time.

Drug metabolismRapid
PoorRapid
CYP2C19 rapid metabolizer · share with your prescriber
Ask anything about your DNA…

The difference

“This sounds like 23andMe?”

Not even close. We sequence your whole genome.

Percentage of your genome read

Lifecode1100%
23andMe<0.1%
Ancestry<0.1%
Other tests<0.1%

1 Whole-genome sequencing, CLIA/CAP certified.

Your genome · 20,000+ genes

High confidencePartial confidenceUncharacterized

Confidence scored against ClinVar

Even the parts we don't understand yet.

So we can let you know when we do.

Last re-analyzed

6 days ago

4 new
BeneficialNew

You likely respond unusually well to beetroot

A regulatory variant lowers your eNOS expression, so dietary nitrate before endurance work boosts blood flow more than average.

NOS3 · regulatory

Re-analyzed with Evo2

Lifecode Health, Inc.

Public Benefit Corporation

Charter · Article IV

“The Corporation shall not sell, license, or transfer any individual’s genetic data, and shall bind every successor to the same duty.”

And we legally can't sell your data.

Every company promises to protect your data, until a new owner, a bad quarter, an investor, or a big enough offer changes their mind. Lifecode made that impossible.

As a Public Benefit Corporation, we’re legally bound by our charter to put the protection of your genome above profit and shareholder returns.

Selling your genetic data isn’t something we won’t do. It’s something we can’t.

Here’s everything you get.

You can’t change your genes — but you can stop fighting them. Our clinical-grade report and guidance show you how.

Your full report.

20+ sections, thousands of insights. Click any to explore.

  • + 11 more sections

Pharmacogenomics

100+ medications across 23 drug-response genes

CPIC Level A

A closer look

GENE CYP2C19*2 / *2

Metabolizer

Poor
Intermediate
Normal
Rapid
Ultrarapid

Medications it affects

Escitalopram · antidepressantBuilds up

Cleared slowly, so it climbs higher than usual. A lower starting dose may suit you.

Clopidogrel · blood thinnerReduced effect

Barely activated. Worth asking about an alternative like ticagrelor.

Plus a clinician-ready PDF written to share with your doctor.

Will I get my mom’s diabetes?

TCF7L2 +1,239 lociUK Biobank

You carry her TCF7L2 variant, putting you in the top 15% for risk. But it’s very preventable, and carriers like you gain the most from acting early, so even small changes now can meaningfully bend

Ask your genome anything.

Grounded in our own genomics context layer, updated every day.

Manually reviewed

Geneticist

Read by a human, not just a model.

A geneticist personally reviews and signs off on your results.

Connects to everything you already wear.

Sync Oura, Whoop, Garmin, Apple Watch, Eight Sleep, Strava and more. Your DNA, in context.

FIG / VAULTENCRYPTED

Yours alone.

Never sold. Delete anytime.

New finding6 days ago

You respond unusually well to zone-2 cardio

PPARGC1A · re-analyzed with Evo2

It keeps getting smarter.

We re-read your genome as the science advances.

~/lifecode

$ lifecode mcp add

✓ available in Claude Code · Cursor · Codex · Opencode

› what raises my heart disease risk?

⏺ polygenic_risk("coronary_artery_disease")

⎿ 92nd percentile · 1,240 variants

Built for developers

An MCP, CLI, and API to build on your genome, in any agent.

Order your genome.

Sequenced once. Yours to keep forever.

  • 100% of your genome sequenced
  • Reports across every category
  • Your raw data, yours forever
  • A painless 15-second swab
Order your genome · $299

one-time payment · free shipping

What happens next

  1. Order kitShips free
  2. Return samplePrepaid label
  3. Results ready~5 weeks
The greatest book ever written is the one hidden in our DNA.
Spencer Wells

Spencer Wells

Harvard Geneticist | Led the Genographic Project , one of the largest surveys of human DNA ever.

Frequently asked questions

What do I get with Lifecode?

We sequence your whole genome (all 6.4 billion base pairs) and turn it into clear, AI-powered insights across disease risk, traits, nutrition, fitness, and medication response. You can also chat with your DNA to explore any of it in plain language.

How is this different from tests like 23andMe or Ancestry?

Those are genotyping arrays that read less than 0.1% of your genome. Lifecode sequences 100% of it — all 6.4 billion base pairs — so you get far more, and far more reliable, signal.

How do I take the test?

It's a painless 15-second cheek swab you do at home: no blood, no clinic, no appointment. Drop the kit in the prepaid mailer and the lab takes it from there.

How long until I get my results?

Sequencing and analysis usually take a few weeks after your sample reaches the lab. We'll email you as soon as your insights are ready.

How accurate are the results?

Your sample is sequenced by CLIA-certified partner labs across your entire genome, not the fraction of it a consumer genotyping array reads.

What happens to my sample and data?

Your sample is inspected, handled under strict protocols, and securely destroyed after sequencing. Your genomic data is encrypted, never sold, and you can delete it at any time.

Can I download my raw DNA data?

Yes. Your whole-genome data belongs to you. Download the raw files whenever you want and take them anywhere.

Will my insights improve over time?

Yes. Because we store your full genome, new insights are added as the science advances. No new sample required.

Is Lifecode a medical diagnosis?

No. Lifecode provides educational, personalized insights to inform conversations with your doctor. It isn't a substitute for professional medical advice or diagnosis.