An estimated 1–2% of the population (3.3-6.6 million people) carry a pathogenic or likely pathogenic (P/LP) variant in one of the genes underlying the following conditions:
- Hereditary breast and ovarian cancer syndrome (HBOC)
- Lynch syndrome (LS)
- Familial hypercholesterolemia (FH)
These hereditary conditions can increase the risk of certain cancers or cardiovascular disease. Inherited disease screening can help your people learn more about their risk for these conditions, enabling them to seek advice, take preventive measures, and facilitate early detection, which can lower costs and improve outcomes. Get the eBook to learn more.