The Inhera family of tests look for inherited genetic variants linked to an increased risk for developing certain types of cancer or disease.

Precision Genomics performs clinical confirmation and cascade testing for known familial variants for common cancer-causing mutations, as well as testing for hereditary causes of ataxia.  

Paired with genetic counseling, this information can help you and your provider develop a personalized plan of care that can often help reduce your risk or detect cancer and disease at an earlier, more treatable stage. 

Inherited risk information is also useful for informing at-risk family members.