Prior Auth Required

0267U - and whole genome sequencing

This procedure appears on the selected insurer prior authorization source.

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Procedure / Serviceand whole genome sequencing
Procedure / Service Description

Rare constitutional and other heritable disorders, identification of copy number variations, - Rare constitutional and other heritable disorders, identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping 0267U and whole genome sequencing Implantation or replacement of carotid sinus baroreflex activation device; pulse generator only 0268T (includes intra-operative interrogation, programming, and repositioning, when performed)

Likely documents
  • Confirm benefit details
  • Submit clinical notes if requested by the plan
Next actions
  • Confirm the current plan policy before submission.
  • Use the insurer authorization workflow for this listed code.