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81414 - Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT

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Procedure / ServiceCardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - sequence analysis panel, must include sequencing of at least 10 genes, including ANK2, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, and SCN5A 81414 Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia); Genetic and Molecular Testing Medical Necessity Guideline

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.