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1298C - Analysis, Common Variants (Eg, 677T, )

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Procedure / ServiceAnalysis, Common Variants (Eg, 677T, )
Procedure / Service Description

zygosity in multiple birth pregnancies) (List separately in addition to code for primary - 81290 2A>G, Del6.4Kb) Mthfr (5,10-Methylenetetrahydrofolate Reductase) (Eg, Hereditary Hypercoagulability) Gene 81291 Analysis, Common Variants (Eg, 677T, 1298C) Mlh1 (Mutl Homolog 1, Colon Cancer, Nonpolyposis Type 2) (Eg, Hereditary Non-Polyposis 81292 Colorectal Cancer, Lynch 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.