Prenatal CHD7 Gene Sequencing (CHARGE Syndrome)
New York
Approved
Genes
Conditions
- CHARGE Syndrome
Clinical Utility
- Full gene sequencing for fetuses with prenatal ultrasound findings suggestive of CHARGE syndrome
- Mutation-specific testing is available via test code 902 for fetuses with a family history of a known mutation
Lab Method
- Capillary Sequencing
Test Code
2262
CPT Codes*
81407x1
ABN Required
No
Turnaround Time**
2-3 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