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81300 - Syndrome) Gene Analysis; Duplication/Deletion Variants

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Procedure / ServiceSyndrome) Gene Analysis; Duplication/Deletion Variants
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81299 Syndrome) Gene Analysis; Known Familial Variants Msh6 (Muts Homolog 6 [E. Coli]) (Eg, Hereditary Non-Polyposis Colorectal Cancer, Lynch 81300 Syndrome) Gene Analysis; Duplication/Deletion Variants Microsatellite instability analysis (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) of markers for mismatch repair deficiency (eg, BAT25, BAT26), includes

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.