Many patients are unaware of their genetic risks for developing common diseases. Clinical-grade polygenic testing is capable of identifying more at-risk individuals than the current standard of care, which relies on assessing for a family history of the disease and occasional testing for rare pathogenic mutations. Our Lifetime Genomics Risk Assessment gives your physician precise information supported by medical evidence to guide personalized health management plans that can help lower your environmental risk of developing the conditions we test for.
Family history, the current standard of care for early risk assessment, can often be unreliable or clinically inaccurate. This means you could be missing information you need to better calculate risk and help your patients prioritize necessary lifestyle changes. Go beyond the standard guidelines to more accurately identify hereditary risk with a simple & convenient blood or saliva sample. Our test is backed by substantial evidence and we support your clinical team with expertly curated education, training, and other resources to help seamlessly integrate genomics into your clinic.
