OncoGeneDx Custom Panel

New York
Approved

Conditions

  • Colorectal Cancer
  • Endometrial Cancer
  • Familial Adenomatous Polyposis (FAP)
  • Lynch Syndrome
  • Ovarian Cancer
  • Pancreatic Cancer
  • Paraganglioma
  • Pheochromocytoma
  • Renal Cancer
  • Attenuated Familial Adenomatous Polyposis (AFAP)
  • Thyroid Cancer
  • Brain Cancer
  • Breast Cancer

Clinical Utility

  • Identify the genetic basis of cancer for individuals who have features and/or a family history consistent with one of the hereditary cancer syndromes described above
  • Determine appropriate clinical management recommendations based on a molecular diagnosis
  • Identify family members at-risk to develop features associated with a specific hereditary cancer syndrome.

Lab Method

  • Deletion/Duplication Analysis
  • Next-Gen Sequencing
  • MLPA

Test Code

B749

CPT Codes*

Varies by Gene

ABN Required

No

Turnaround Time**

21 days

Preferred Specimen

2-5 mL Blood - Lavender Top Tube

Alternative Specimen

Buccal Swabs | Fibroblasts (separate charge for cell culture may apply)

*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.

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