The Single-Gene Risk test identifies genetic variants associated with health conditions, including cancer, cardiovascular diseases, and other health-related conditions. This test provides providers and patients with insights for proactive health management through early detection of variants shown to cause disease, personalized care, and risk stratification.





The Single-Gene Risk test helps healthy adults gain genetic insights, even without a strong personal or family history. It is not intended for diagnosing conditions based on family or personal history.
PR21037
(Single-Gene Risk, Proactive Health Plus - 151 Genes)
PR22020
(Single-Gene Risk, Proactive Health - 84 Genes)
From samples received, most results are delivered in 5 to 6 weeks*.
If you've already had MyOme testing performed, follow-up testing or re-requisitions are typically completed in under 2 weeks, often within just a few days.
A comprehensive screening of 151 genes using 30x whole-genome sequencing, providing the ability for reanalysis and updated genetic information than panel based approaches or exomes.

A more affordable option that screens 84 genes using high-coverage exome plus low-coverage WGS —offering a cost-effective option for preventative health decisions.



Patients with a personal or family history of a condition tested in the Single-Gene Risk test may need further screening or genetic testing.
The test is a screening tool and should not be used by those diagnosed with disease. A negative result doesn't eliminate the risk of developing a condition. MyOme offers genetic counseling to help with risk assessment and management.
Get more information on how to order a MyOme test and get the process started.
