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Short term offer: take this test now and save $150
Shop now →Physician-reviewed with online consultation. Combine genetics, health history and lifestyle. Prevent don't treatPrevent, don't treat.
100% HSA /
FSA Eligible
Results in 4–6 weeks from purchase
Your DNA stays yours.: encrypted, never sold, and you can request deletion. Privacy Policy
80%
of heart attacks are preventable
5
conditions assessed in one test
1M+
genetic variants analyzed
The benefits
Understand your heart and metabolic disease predispositions, holistically
Consult with a licensed physician
Focus your longevity plan on what matters most to you personally
Make informed decisions with your physician about lifestyle changes and preventive medications, such as statins, blood pressure medications, and smoking cessation drugs
Know your predisposition to obesity to make better decisions about GLP-1 weight-loss medications
Use your polygenic and clinical data to better understand your risks and build a targeted prevention plan
Understand your genetic risk for common conditions and take proactive steps for better health and condition prevention. This at-home test analyzes your DNA to provide personalized risk insights reviewed by certified physicians.
Simple. Accurate. From the comfort of your home.
Short term offer — limited time only
Your DNA stays yours.: encrypted, never sold, and you can request deletion. Privacy Policy

Your report
Your report translates complex polygenic data into plain-language explanations your doctor can act on immediately.
Polygenic + clinical risk scores
Our models combine your genetic variants with clinical factors for more accurate prediction than genetics or bloodwork alone.
Physician consultation included
Your consultation with a licensed physician is included. They review your results and build a personalized prevention plan with you.
Physician-ready PDF
Share a clinician-formatted version of your results directly with your GP or cardiologist to start the conversation.
Interactive risk explorer
Through your personal portal, explore how lifestyle changes — quitting smoking, increasing exercise, adjusting weight, blood pressure, or cholesterol — interactively shift your risk level in real time.

What our customers say
“It gave me another piece of information to help me have a better conversation with my doctor.”
OpenDNA customer
Customer experience, not medical advice.
Your DNA stays yours.: encrypted, never sold, and you can request deletion. Privacy Policy
The research
Our coronary artery disease model is built on peer-reviewed research and validated in a large population cohort. Each risk score is calibrated to reflect your risk relative to the general population, giving you a meaningful benchmark for proactive action.
Explore the research behind our models


Simple process
From swab to personalized action plan — all from home, supported by a board-certified physician licensed in your state.
01
Order online
Choose your test; a physician consultation is included. Kit ships to your door in 2–3 days.
02
Collect your sample
A simple cheek swab at home — no needles, no clinic visit. Register your kit online and mail it back in the prepaid envelope.
03
Model analysis
Our platform analyzes over one million genetic variants using polygenic risk scores combined with your clinical profile. Results in 4–6 weeks from purchase.
04
Your personalized report
Access your full report and your included consultation with a licensed physician to discuss your results and next steps.
What we assess
Our test goes far beyond cholesterol checks, assessing your polygenic risk across the full cardiometabolic spectrum.
Heart disease

Type 2 diabetes
Hypertension

High cholesterol
Obesity
Heart disease

Type 2 diabetes
Hypertension

High cholesterol
Obesity
80%
of heart attacks are preventable with early identification and proactive care.
Source: American College of Cardiology, 2023
See the science behind our test →We analyze over one million genetic variants across your DNA, combined into polygenic risk scores — a measure of your individual genetic tendency for each condition, based on the latest large-scale genomic research.
The science
A PRS estimates an individual's inherited likelihood for a condition by combining the effects of many genetic variants across the genome — capturing cumulative risk that single-gene tests cannot detect.
OpenDNA's models are built on millions of variants drawn from large-scale genomic research, delivering broad population coverage and strong predictive accuracy beyond what any single biomarker can provide.
1M+
Genetic variants analyzed
5
Conditions assessed
500K+
Research participants underpinning our models
"By partnering with OpenDNA, we can now offer genetic screening that empowers our patients to take proactive steps towards managing their health and preventing future illness."
Dr. William Harper
CEO & Founder, Harper Health
Our Mission
Genomic data holds enormous potential for preventing conditions — yet it remains largely absent from everyday clinical decisions. Our mission is to bridge that gap: integrating polygenic and clinical information into unified models that empower individuals and physicians to understand personal health risks and act on them before a condition develops.
What drives us
Genetics at the core
Your DNA carries signals about future health risks that are detectable today. We translate complex genomic science into clear, personalized risk assessments you can act on.
Clinical context matters
Genetic signals become far more powerful when combined with clinical data. Our models integrate both to deliver insights that reflect your full health picture.
Decisions that matter
We aim to help people and their physicians act on risk sooner. In a clinical study, polygenic results influenced physicians' care decisions.
We believe earlier, more personalized risk insight can help people and their physicians prevent disease sooner.
Our expertise
Our team brings together deep expertise in genomics and clinical medicine — united by a shared goal of transforming how cardiometabolic disease risk is assessed, communicated, and managed.

Personalized prevention for everyone