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81328 - SLCO1B1 (solute carrier organic anion transporter family, member 1B1) (eg, adverse

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Procedure / ServiceSLCO1B1 (solute carrier organic anion transporter family, member 1B1) (eg, adverse
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - neuropathy with liability to pressure palsies) gene analysis; known familial variant 81327 SEPT9 (Septin9) (eg, colorectal cancer) promoter methylation analysis 81328 SLCO1B1 (solute carrier organic anion transporter family, member 1B1) (eg, adverse drug reaction), gene analysis, common variant(s) (eg, *5) 81329 SMN1 (survival of motor neuron 1, telomeric) (eg, spinal muscular atrophy) gene

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.