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81270 - Variant

This procedure appears on the selected insurer prior authorization source.

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Procedure / ServiceVariant
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81269 syndrome, HbH disease), gene analysis; duplication/deletion variants Jak2 (Janus Kinase 2) (Eg, Myeloproliferative Disorder) Gene Analysis, P.Val617Phe (V617F) 81270 Variant HTT (huntingtin) (eg, Huntington disease) gene analysis; evaluation to detect abnormal (eg, 81271 expanded) alleles

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.