Forms and Documents
- For smaller custom gene lists of 2-150 genes
- For analysis of genes within regions of homozygosity detected by whole genome array
- Identification of underlying molecular cause of clinical diagnosis
- Recurrence risk assessment
- Next-Gen Sequencing
*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.