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81330 - Type A) Gene Analysis, Common Variants (Eg, R496L, L302P, Fsp330)

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Procedure / ServiceType A) Gene Analysis, Common Variants (Eg, R496L, L302P, Fsp330)
Procedure / Service Description

dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, - 81329 centromeric) analysis, if performed Smpd1(Sphingomyelin Phosphodiesterase 1, Acid Lysosomal) (Eg, Niemann-Pick Disease, 81330 Type A) Gene Analysis, Common Variants (Eg, R496L, L302P, Fsp330) Snrpn/Ube3A (Small Nuclear Ribonucleoprotein Polypeptide N And Ubiquitin Protein Ligase 81331 E3A) (Eg, Prader-Willi Syndrome And/Or Angelman Syndrome), Methylation Analysis

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.