81295 Msh2 gene full seq
Also known as: MSH2 full sequencing, MSH2 complete analysis
Mutator S Homolog 2 (MSH2) gene full gene sequence analysis to identify all variant types causing Lynch syndrome and hereditary cancer.
In Plain Language
Complete colorectal cancer genetic test; Full Lynch syndrome screening
Clinical Context
Complete MSH2 sequencing for Lynch syndrome diagnosis, especially in families with early-onset colorectal and endometrial cancers.
RVU Information
CPT 81295 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81295?
CPT 81295 (Msh2 gene full seq) is a Pathology & Lab code. Mutator S Homolog 2 (MSH2) gene full gene sequence analysis to identify all variant types causing Lynch syndrome and hereditary cancer.
Who uses CPT code 81295?
CPT 81295 is used by Pathology, Oncology, Gastroenterology. Complete MSH2 sequencing for Lynch syndrome diagnosis, especially in families with early-onset colorectal and endometrial cancers.
When is CPT 81295 used?
Complete MSH2 sequencing for Lynch syndrome diagnosis, especially in families with early-onset colorectal and endometrial cancers.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.