Prior Auth Required

81348 - myeloid leukemia) gene analysis, common variants (eg, P95H, P95L)

This procedure appears on the selected insurer prior authorization source.

Check another codeExplore policy data
Prior authorizationPrior Auth Required
Procedure / Servicemyeloid leukemia) gene analysis, common variants (eg, P95H, P95L)
Procedure / Service Description

dosage/deletion analysis (eg, carrier testing), includes SMN2 (survival of motor neuron 2, - 81347 leukemia) gene analysis, common variants (eg, A672T, E622D, L833F, R625C, R625L) SRSF2 (serine and arginine-rich splicing factor 2) (eg, myelodysplastic syndrome, acute 81348 myeloid leukemia) gene analysis, common variants (eg, P95H, P95L) Cytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities; interrogation of genomic regions for copy number and loss-of-heterozygosity variants, low-

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.