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81320 - common variants (eg, R665W, S707F, L845F)

This procedure appears on the selected insurer prior authorization source.

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Procedure / Servicecommon variants (eg, R665W, S707F, L845F)
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 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) PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor 81321 syndrome) gene analysis; full sequence analysis

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.