Your Privacy Choices

We use cookies for analytics and ads, never on health pages.We use cookies to understand how visitors use our public pages and to measure ad performance — never on pages with your health information. Privacy Policy

Our science

Where genomics and clinical medicine meet

OpenDNA combines cutting-edge polygenic science with clinical data integration to deliver risk insights that are more accurate, more personalized, and more actionable than any single source of data alone.Polygenic science plus clinical data for more accurate insights.

01

Polygenic Risk Scores (PRS)

Unlike single-gene tests, our polygenic models analyze over one million genetic variants or SNPs (Single Nucleotide Polymorphisms) simultaneously. This captures the cumulative effect of your entire genome on condition risk, rather than the contribution of a single gene.We analyze over one million genetic variants (SNPs) at once.

For coronary artery disease, a model combining a polygenic score with clinical data identified more at-risk adults than the standard clinical risk calculator. Read the study →

Polygenic Risk Scores (PRS)

02

Clinical data integration

Genetic signals become far more powerful when combined with clinical measurements. Our models integrate your genetic profile with clinical and lifestyle factors — delivering a complete, personalized risk picture based on both your genetic and clinical profile.We combine your genetics with clinical and lifestyle factors.

Clinical data integration

03

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.Peer-reviewed; our coronary artery disease model is validated in a large cohort.

Explore the research behind our modelsOur research

BMC Medical GenomicsFrontiers in Genetics
Peer-reviewed research
OpenDNA poster presented at ACC 2025

04

Physician-reviewed insights

Every report is reviewed and signed by a board-certified physician licensed in your state. Our clinical team ensures that insights are medically accurate, contextually relevant, and actionable — not just a data printout.Every report is signed by a board-certified physician licensed in your state.

Physician-reviewed insights

The evidence

What the published studies show

BMC Medical Genomics, 2025

Coronary artery disease risk prediction

A model combining a polygenic risk score with clinical factors identified more at-risk adults than the standard clinical risk calculator.

Read the study →

Frontiers in Genetics, 2025

Polygenic scores and physician decision-making

In a clinical study of patients, polygenic results influenced physicians' management decisions, most often patient education and monitoring.

Read the study →

Both studies were funded by OpenDNA, and some of the authors are OpenDNA employees.

"Genetics alone isn't enough. The future of preventive medicine combines your DNA with who you are clinically — and what you can change.""Genetics alone isn't enough. Prevention combines your DNA with who you are clinically."

OpenDNA Science Team