SLC22A5 Gene Sequencing & Del/Dup
New York
Approved
Genes
Conditions
- Primary/Systemic Carnitine Deficiency
Clinical Utility
- Confirmation of biochemical diagnosis
- To confirm maternal PCD
- Carrier testing
Lab Method
- Next-Gen Sequencing
- Deletion/Duplication Analysis
Test Code
365
CPT Codes*
81405x1
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.
**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.
Billing
Targeted Variant Testing