APOB, LDLR, LDLRAP1, PCSK9
- Familial Hypercholesterolemia
- Molecular confirmation of a clinical diagnosis in symptomatic individuals
- Risk assessment of asymptomatic family members of a proband diagnosed with FH
- Differentiation of FH from acquired (non-genetic) forms of hypercholesterolemia
- Genetic counseling and recurrence risk assessment
- Deletion/Duplication Analysis
- Next-Gen Sequencing
81405x1, 81406x2, 81407x1, 81479x1
*The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
**Turnaround times are estimates and begin once the sample(s) begin processing at the GeneDx lab and could be extended in situations outside GeneDx’s control.
Targeted Variant Testing