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81337 - known familial sequence variant(s)

This procedure appears on the selected insurer prior authorization source.

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Procedure / Serviceknown familial sequence variant(s)
Procedure / Service Description

dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, - 81336 gene sequence SMN1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene analysis; 81337 known familial sequence variant(s) MPL (MPL proto-oncogene, thrombopoietin receptor) (eg, myeloproliferative disorder) gene 81338 analysis; common variants (eg, W515A, W515K, W515L, W515R)

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.