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81319 - Colorectal Cancer, Lynch Syndrome) Gene Analysis; Duplication/Deletion Variants

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Procedure / ServiceColorectal Cancer, Lynch Syndrome) Gene Analysis; Duplication/Deletion Variants
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81318 Colorectal Cancer, Lynch Syndrome) Gene Analysis; Known Familial Variants Pms2 (Postmeiotic Segregation Increased 2 [S. Cerevisiae]) (Eg, Hereditary Non-Polyposis 81319 Colorectal Cancer, Lynch Syndrome) Gene Analysis; Duplication/Deletion Variants PLCG2 (phospholipase C gamma 2) (eg, chronic lymphocytic leukemia) gene analysis, 81320 common variants (eg, R665W, S707F, L845F)

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.