Prior Auth Required

81449 - sequence variants and copy number variants or rearrangements, if performed; RNA analysis

This procedure appears on the selected insurer prior authorization source.

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Procedure / Servicesequence variants and copy number variants or rearrangements, if performed; RNA analysis
Procedure / Service Description

Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish- - 81448 genes (eg, BSCL2, GJB1, MFN2, MPZ, REEP1, SPAST, SPG11, SPTLC1) Solid organ neoplasm, genomic sequence analysis panel, 5-50 genes, interrogation for 81449 sequence variants and copy number variants or rearrangements, if performed; RNA analysis Hematolymphoid neoplasm or disorder, genomic sequence analysis panel, 5-50 genes, interrogation for sequence variants, and copy number variants or rearrangements, or isoform

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.