81297 Msh2 gene dup/delete variant
Pathology & Lab
Also known as: MSH2 copy number analysis, MSH2 deletion duplication testing
Mutator S Homolog 2 (MSH2) gene duplication and deletion variant analysis to detect copy number variations in Lynch syndrome.
Clinical Context
Identifies MSH2 deletions and duplications to improve diagnostic yield in suspected Lynch syndrome when sequencing is negative.
RVU Breakdown
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| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
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Specialties
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