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81327 - SEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis

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Procedure / ServiceSEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - PMP22 (peripheral myelin protein 22) (eg, Charcot-Marie-Tooth, hereditary neuropathy with 81326 liability to pressure palsies) gene analysis; known familial variant 81327 SEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis SLCO1B1 (solute carrier organic anion transporter family, member 1B1) (eg, adverse drug 81328 reaction), gene analysis, common variant(s) (eg, *5)

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.