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Your DNA holds
the answers

Millions live with undiagnosed chronic conditions. We decode your unique genomic vulnerabilities and create personalized supplements that target exactly what your body needs.

It's not magic, it's the future of medicine.

Built on research from leading institutions

Stanford MedicineMayo ClinicNature GeneticsNIHHarvard Medical23andMe ResearchStanford MedicineMayo ClinicNature GeneticsNIHHarvard Medical23andMe ResearchStanford MedicineMayo ClinicNature GeneticsNIHHarvard Medical23andMe ResearchStanford MedicineMayo ClinicNature GeneticsNIHHarvard Medical23andMe Research
25M+Americans with undiagnosed conditions
7.6Average years to get diagnosed
93%Of DNA variants go unexamined
47%Report supplement deficiencies

The Science

Built on genomic intelligence,
not guesswork

Traditional medicine treats symptoms. We treat the root cause encoded in your DNA — using the most advanced science available.

Genomic Sequencing

We analyze over 700,000 genetic markers from a simple saliva sample, mapping your unique biological blueprint with clinical-grade precision.

AI-Driven Analysis

Our proprietary algorithms cross-reference your genetic data against the latest peer-reviewed research to identify metabolic vulnerabilities.

Precision Formulation

Each supplement blend is compounded specifically for your genome — the exact micronutrients, at the exact doses your body actually needs.

Clinical Validation

Every formulation is validated against known genomic pathways and reviewed by our medical advisory board before shipping to you.

Your Genomic Map

We find what others miss

A glimpse at how we map your genomic vulnerabilities to create your personalized supplement protocol.

MTHFR C677T

Folate Metabolism

Action needed

VDR Bsm1

Vitamin D Receptor

Action needed

COMT Val158Met

Methylation

Optimal

CYP1B1 rs1056836

Estrogen Metabolism

Action needed

SOD2 A16V

Antioxidant Defense

Optimal

FUT2 G772A

B12 Absorption

Action needed

CYP1A2 rs762551

Caffeine Metabolism

Optimal

NBPF3 rs4654748

B6 Processing

Action needed

TCN2 rs1801198

B12 Transport

Action needed

BCMO1 rs7501331

Beta-Carotene Conversion

Optimal

SLC23A1 rs33972313

Vitamin C Transport

Optimal

GC rs2282679

Vitamin D Binding

Action needed

PEMT rs7946

Choline Synthesis

Action needed

CBS rs234706

Homocysteine Clearance

Optimal

NOS3 rs1799983

Nitric Oxide Production

Action needed

MTRR A66G

Methionine Synthase

Action needed

MAO-A rs6323

Serotonin Breakdown

Optimal

GAD1 rs3791878

GABA Synthesis

Action needed

FADS1 rs174546

Omega-3 Conversion

Action needed

SLC30A8 rs13266634

Zinc Transport

Optimal

HFE C282Y

Iron Regulation

Action needed

CYP2D6 rs3892097

Drug Metabolism

Optimal

TNF-a rs1800629

Inflammation Response

Action needed

IL-6 rs1800795

Cytokine Signaling

Action needed

APOE rs429358

Lipid Metabolism

Optimal

MTR A2756G

Methionine Recycling

Action needed

AHCY rs819147

SAH Hydrolysis

Optimal

SHMT1 rs1979277

Folate Cycling

Action needed

DHFR rs70991108

Folate Reduction

Optimal

SLC19A1 rs1051266

Folate Transport

Action needed

PON1 Q192R

Detoxification

Action needed

GPX1 rs1050450

Glutathione Peroxidase

Optimal

CAT rs1001179

Catalase Activity

Action needed

GST-M1 deletion

Phase II Detox

Action needed

NAT2 rs1208

Acetylation Capacity

Optimal

CLOCK rs1801260

Circadian Rhythm

Optimal

ADA rs73598374

Adenosine Metabolism

Action needed

BDNF Val66Met

Neuroplasticity

Action needed

DIO2 rs225014

Thyroid Conversion

Action needed

SLC6A4 5-HTTLPR

Serotonin Reuptake

Optimal

Analysis Summary

24variants detected

24 of 40 markers require intervention

Flagged Variants (24)

MTHFR C677T

Folate Metabolism

TARGET

VDR Bsm1

Vitamin D Receptor

TARGET

CYP1B1 rs1056836

Estrogen Metabolism

TARGET

FUT2 G772A

B12 Absorption

TARGET

NBPF3 rs4654748

B6 Processing

TARGET

TCN2 rs1801198

B12 Transport

TARGET

GC rs2282679

Vitamin D Binding

TARGET

PEMT rs7946

Choline Synthesis

TARGET

NOS3 rs1799983

Nitric Oxide Production

TARGET

MTRR A66G

Methionine Synthase

TARGET

GAD1 rs3791878

GABA Synthesis

TARGET

FADS1 rs174546

Omega-3 Conversion

TARGET

HFE C282Y

Iron Regulation

TARGET

TNF-a rs1800629

Inflammation Response

TARGET

IL-6 rs1800795

Cytokine Signaling

TARGET

MTR A2756G

Methionine Recycling

TARGET

SHMT1 rs1979277

Folate Cycling

TARGET

SLC19A1 rs1051266

Folate Transport

TARGET

PON1 Q192R

Detoxification

TARGET

CAT rs1001179

Catalase Activity

TARGET

GST-M1 deletion

Phase II Detox

TARGET

ADA rs73598374

Adenosine Metabolism

TARGET

BDNF Val66Met

Neuroplasticity

TARGET

DIO2 rs225014

Thyroid Conversion

TARGET

Scroll to see all flagged variants

How It Works

From saliva to solution
in four simple steps

Step 01Results in 2-3 weeks

Saliva Test

We send you a simple at-home saliva collection kit. No needles, no doctor visits. Just spit, seal, and ship.

Step 02700K+ markers analyzed

Genomic Analysis

Our AI scans 700,000+ genetic markers, cross-referencing with the latest research on metabolic pathways and nutrient processing.

Step 03Precision-compounded

Custom Supplements

We formulate a personalized supplement blend targeting your specific deficiencies — compounded just for you.

Step 04Continuous optimization

Track Progress

Monitor your biomarkers over time, with quarterly reassessments to optimize your formulation as your health improves.

Real Results

Lives transformed by
precision genomics

89%

Report significant improvement within 90 days

4.9/5

Average satisfaction rating from beta users

3.2x

More effective than generic supplement stacks

"After 12 years of doctors telling me nothing was wrong, undiagnosed.ai found three methylation pathway variants. Six weeks on my custom blend and I feel like a different person."

Sarah M.

Chronic fatigue

82% symptom reduction

"I was skeptical — I'd tried every supplement on the shelf. But when the formulation is actually designed for YOUR genome, the difference is night and day."

James K.

Brain fog & joint pain

Symptom-free in 3 months

"The genetic report alone was worth it. For the first time, I understood WHY my body wasn't processing B12 properly. The supplements were the solution I'd been searching for."

Dr. Priya L.

Nutrient malabsorption

Lab values normalized

The Science

This isn't another DNA gimmick.

Our lab conducts original genetic research never previously applied to chronic illness. Here's how it works.

Join the Future

Your genome is waiting
to be decoded

Be among the first to experience DNA-powered personalized medicine. Early members get priority access and founding member pricing.

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