Prior Auth Required

81333 - common variants (eg, R124H, R124C, R124L, R555W, R555Q)

This procedure appears on the selected insurer prior authorization source.

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Prior authorizationPrior Auth Required
Procedure / Servicecommon variants (eg, R124H, R124C, R124L, R555W, R555Q)
Procedure / Service Description

dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, - 81332 (eg, alpha-1-antitrypsin deficiency), gene analysis, common variants (eg, *S and *Z) TGFBI (transforming growth factor beta-induced) (eg, corneal dystrophy) gene analysis, 81333 common variants (eg, R124H, R124C, R124L, R555W, R555Q) RUNX1 (runt related transcription factor 1) (eg, acute myeloid leukemia, familial platelet disorder with associated myeloid malignancy), gene analysis, targeted sequence analysis (eg,

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.