Prior Auth Required

81332 - (eg, alpha-1-antitrypsin deficiency), gene analysis, common variants (eg, *S and *Z)

This procedure appears on the selected insurer prior authorization source.

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Procedure / Service(eg, alpha-1-antitrypsin deficiency), gene analysis, common variants (eg, *S and *Z)
Procedure / Service Description

dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, - 81331 E3A) (Eg, Prader-Willi Syndrome And/Or Angelman Syndrome), Methylation Analysis SERPINA1 (serpin peptidase inhibitor, clade A, alpha-1 antiproteinase, antitrypsin, member 1) 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)

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.