Unlock your genetic health potential. GeneHealth analyzes 95+ genetic markers across six critical health categories — from cardiovascular and metabolic health to longevity and organ function — giving you the most comprehensive health genetic profile available.
Comprehensive analysis of genes that influence your overall health, wellness, and longevity
Unlock deep insights into your genetic predispositions across six critical health categories
Analyze genes affecting heart health, cholesterol metabolism, blood pressure regulation, and vascular function.
Studies show that individuals with favorable APOE variants have up to 40% lower cardiovascular disease risk compared to ε4 carriers.

Our CLIA-certified laboratory uses MassArray Technology to deliver the most comprehensive health genetic insights available.
The questions you've Googled a hundred times — finally answered by the one thing that's been there all along

Genetics explain why. The APOE, PCSK9, and CETP genes control how your liver processes cholesterol — and some variants mean your body overproduces it regardless of diet. Up to 1 in 5 people have a genetic variant that makes cholesterol nearly impossible to manage with lifestyle alone.
Statin therapy + reduced saturated fat dramatically lowers cardiovascular risk even with this variant
Real people who stopped guessing and started knowing — and what changed when they did

“My cardiologist kept telling me my cholesterol was "borderline" — eat less fat, exercise more. I did everything right for 3 years. Nothing changed. GeneHealth found an APOE ε3/ε4 variant. That single discovery changed everything. My doctor finally understood why diet wasn't working, started me on the right statin dose, and my LDL dropped 47% in 90 days.”
“I'd been diagnosed with 'generalized anxiety' and chronic fatigue for 6 years. Four therapists, two SSRIs, nothing really worked. GeneHealth found a compound MTHFR mutation — C677T and A1298C. My psychiatrist had never tested for it. Three weeks on methylfolate and B12, the brain fog lifted. I feel like myself for the first time in years.”
“My father died of a heart attack at 61. My brother had a bypass at 57. I assumed it was my future too. GeneHealth showed I actually carry the FOXO3 longevity variant — and that while I did inherit an ACE risk allele from my dad, my protective SIRT1 genes counterbalance it substantially. I'm not off the hook, but I'm not destined for their outcome either.”
Select the plan that best fits your health goals
$125 one-time kit fee
Perfect for individuals starting their health journey
$125 one-time kit fee
Most comprehensive health genetic analysis
$125 one-time kit fee
Complete health solution for your whole family
Explore a detailed sample report to understand the comprehensive insights you'll receive
Genetic analysis and personalized recommendations
The APOE ε4 allele is associated with increased cardiovascular disease risk and altered cholesterol metabolism. Carriers may benefit from enhanced dietary fat management and regular cardiovascular monitoring.
Focus on Mediterranean diet patterns, omega-3 supplementation (2-3g daily), and regular lipid panel monitoring every 6 months.
This variant reduces MTHFR enzyme activity by approximately 35%, affecting homocysteine metabolism and cardiovascular health. Elevated homocysteine is a known cardiovascular risk factor.
Supplement with methylated B vitamins (methylfolate 800mcg, methylcobalamin 1000mcg daily) and monitor homocysteine levels annually.
Heterozygous ACE insertion/deletion variant shows balanced cardiovascular response. No significant increased risk for hypertension or cardiac events.
Maintain standard cardiovascular health practices including regular exercise and blood pressure monitoring.
Normal NOS3 variant supports optimal nitric oxide production and vascular health. This is associated with better endothelial function and cardiovascular protection.
Support nitric oxide pathways with dietary nitrates (leafy greens, beets) and regular aerobic exercise.
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Comprehensive foundational genetic testing covering essential health markers and disease risk factors
Four simple steps. No clinic visits, no blood draws, no waiting rooms. Just answers.

A beautifully packaged collection kit arrives at your door with everything you need: a sealed cheek swab, prepaid return envelope, and step-by-step instructions. Free shipping, both ways.
Just swab the inside of your cheek for 30 seconds per side, seal it in the provided tube, and drop it in your prepaid return envelope. That's it. Most people do it before their morning coffee.
Our CLIA-certified laboratory analyzes 95+ genes using Illumina MassArray sequencing technology — the same platform used in leading academic medical centers. Every result goes through two independent quality reviews before leaving the lab.
You receive a beautifully designed, clinically actionable report covering all 6 health categories. Share it directly with your doctor, or schedule a session with one of our board-certified genetic counselors who'll walk you through every finding.
Join 50,000+ people who stopped guessing about their health and started acting on answers only their DNA could give them.
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