Forms and Documents
- Carrier testing for a specific mutation previously identified in a family.
- Clinical laboratory confirmation of one or more mutations identified in a research laboratory
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
**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.