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81289 - FXN (frataxin) (eg, Friedreich ataxia) gene analysis; known familial variant(s)

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Procedure / ServiceFXN (frataxin) (eg, Friedreich ataxia) gene analysis; known familial variant(s)
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - MLH1 (mutL homolog 1, colon cancer, nonpolyposis type 2) (eg, hereditary non-polyposis 81288 colorectal cancer, Lynch syndrome) gene analysis; promoter methylation analysis 81289 FXN (frataxin) (eg, Friedreich ataxia) gene analysis; known familial variant(s) Mcoln1 (Mucolipin 1) (Eg, Mucolipidosis, Type Iv) Gene Analysis, Common Variants (Eg, Ivs3- 81290 2A>G, Del6.4Kb)

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.