81300 Msh6 gene dup/delete variant
Also known as: MSH6 copy number analysis, MSH6 deletion duplication testing
Mutator S Homolog 6 (MSH6) gene duplication and deletion variant analysis to identify copy number variations in Lynch syndrome.
In Plain Language
MSH6 gene copy number test; Lynch syndrome copy variation testing
Clinical Context
Detects MSH6 deletions and duplications to improve diagnostic sensitivity in suspected Lynch syndrome.
RVU Information
CPT 81300 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 81300?
CPT 81300 (Msh6 gene dup/delete variant) is a Pathology & Lab code. Mutator S Homolog 6 (MSH6) gene duplication and deletion variant analysis to identify copy number variations in Lynch syndrome.
Who uses CPT code 81300?
CPT 81300 is used by Pathology, Oncology, Gastroenterology. Detects MSH6 deletions and duplications to improve diagnostic sensitivity in suspected Lynch syndrome.
When is CPT 81300 used?
Detects MSH6 deletions and duplications to improve diagnostic sensitivity in suspected Lynch syndrome.
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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.