Testing whether someone carries a harmful variant in one of these genes can confirm whether a condition is, indeed, the result of an inherited syndrome. Genetic testing is also done to determine whether family members who have not (yet) developed a cancer have inherited the same variant as a family member who is known to carry a harmful (cancer susceptibility predisposing) variant.

Genetic testing for the detection of variants associated with an increased risk of autoimmune diseases that will allow you to know if there are any predispositions or gene mutations for autoimmune disease or deficiency.

Genetic testing is informative and useful for the clinical management of various inherited cardiovascular diseases such as cardiomyopathies, arrhythmic disorders, thoracic aortic aneurysms and dissections, and familial hypercholesterolemia (FH).

Pharmacogenetic (PGx) testing tells you how genetic factors impact your ability to process and respond to medications. It also allows your physician to better prescribe medications to best suit you.

Testing that will allow you to know if you are at risk for developing Alzheimer's, Dementia, Parkinsons, Huntington’s, and 65 other neurocognitive diseases.

Provides focused results for more than 60 genes that have been implicated in inherited (monogenic) lung disease.