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0234U - insertions, and variants in non-uniquely mappable regions

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Procedure / Serviceinsertions, and variants in non-uniquely mappable regions
Procedure / Service Description

guidance, lumbar or sacral; each additional level (List separately in addition to code for - MECP2 (methyl CpG binding protein 2) (eg, Rett syndrome), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element 0234U insertions, and variants in non-uniquely mappable regions PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome), full gene analysis, including small sequence changes in exonic and intronic

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.