Custom Arrhythmia Panel
Conditions
- Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
- Long QT Syndrome (LQTS)
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Short QT Syndrome (SQTS)
- Brugada Syndrome
Clinical Utility
- Molecular confirmation of a clinical diagnosis in symptomatic individuals
- Risk assessment of asymptomatic family members of a proband with arrhythmia
- Differentiation of hereditary arrhythmia from acquired (non-genetic) arrhythmia
- Recurrence risk calculation
Lab Method
- Deletion/Duplication Analysis
- Next-Gen Sequencing
Important Information
Test Code
695C
CPT Codes*
81413x1, 81414x1
ABN Required
No
Turnaround Time**
4 weeks
Preferred Specimen
Alternative Specimen
*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.
**Reporting times are typical and begin once the sample(s) are received at the GeneDx laboratory, but could be extended in situations outside GeneDx’s reasonable control.
Test Documents
Billing
Targeted Variant Testing