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Short term offer: take this test now and save $150

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Go Beyond Genetics.
Get a Personalized Health Plan

Physician-reviewed with online consultation. Combine genetics, health history and lifestyle. Prevent don't treatPrevent, don't treat.

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WHAT'S INCLUDED

At-home test: cheek-swab kit shipped to you and back, freeAt-home kit, shipped free both ways

Genetic predisposition for five conditionsGenetic risk for five conditions

Heart disease

Type 2 diabetes

Obesity

Hypertension

High cholesterol

Combined genetic, clinical and lifestyle risk assessmentCombined genetic, clinical & lifestyle risk assessment

Heart disease

Type 2 diabetes

Personalized report with longevity recommendations and an interactive risk dashboardPersonalized report, longevity recommendations & dashboard

Physician review & consultation

Results in 4–6 weeks from purchase

Learn more →

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

WHAT'S INCLUDED

At-home test: cheek-swab kit shipped to you and back, freeAt-home kit, shipped free both ways

Genetic predisposition for five conditionsGenetic risk for five conditions

Heart disease

Type 2 diabetes

Obesity

Hypertension

High cholesterol

Combined genetic, clinical and lifestyle risk assessmentCombined genetic, clinical & lifestyle risk assessment

Heart disease

Type 2 diabetes

Personalized report with longevity recommendations and an interactive risk dashboardPersonalized report, longevity recommendations & dashboard

Physician review & consultation

Results in 4–6 weeks from purchase

Trusted by Top Clinics

HIPAA Compliant · CLIA/CAP Accredited

LegitScript Certified

80%

of heart attacks are preventable

5

conditions assessed in one test

1M+

genetic variants analyzed

The benefits

Why take the OpenDNA test

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

OpenDNA Health

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

Clear, actionable insights — not just data

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.

CardioRisk results on tablet

What our customers say

A better conversation with your doctor

“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

Built on peer-reviewed 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

BMC Medical GenomicsFrontiers in Genetics
Scientific research
OpenDNA poster presented at ACC 2025

Simple process

Four steps to understanding your heart health

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

5 conditions. One test.

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

What is a Polygenic Risk Score?

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."

WH

Dr. William Harper

CEO & Founder, Harper Health

Our Mission

Bridging the gap between genomics and preventive care

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

The pillars of our approach

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.

Transforming preventive medicine — globally

We believe earlier, more personalized risk insight can help people and their physicians prevent disease sooner.

Our expertise

Where genomics and clinical medicine meet

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.

OpenDNA

Personalized prevention for everyone

© 2026 OpenDNA · Personalized prevention for everyone

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