About 40% of people have an increased risk for at least one common hereditary disease. Clinical-grade polygenic testing is capable of identifying 2-4x more at-risk individuals than assessing for a family history of the disease and sometimes as much as 10x as many individuals compared to those that have testing ordered for rare pathogenic mutations alone. 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 clinical standard of care, is accurately supplied by on average 5-8% of patients. This means you could be missing over 80% of the 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.
