A single test to detect mutations in 84 genes responsible for monogenic diseases of early atherosclerosis . Covered conditions include the following Premature Coronary Artery Disease, Familial Hypercholesterolemia & Familial Triglyceridemia.
|Suitable For:||Individuals who want to know the risk of Premature Coronary Disease, Familial Hypercholesterolemia & Familial Triglyceridemia|
|Lab Certification:||CAP / CLIA|
|TAT:||14 – 21 working days upon receipt of sample at Laboratory|