81296 Msh2 gene known variants
Pathology & Lab
Also known as: MSH2 familial variant testing, MSH2 family screening
Mutator S Homolog 2 (MSH2) gene analysis for known familial variants to facilitate screening of family members with Lynch syndrome.
Clinical Context
Targeted MSH2 testing of family members for previously identified variants. Streamlines diagnosis and cancer surveillance planning in families.
RVU Breakdown
| Work RVU | 0.00 |
| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
| Total RVU | 0.00 |
Specialties
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