81299 Msh6 gene known variants
Also known as: MSH6 familial variant testing, MSH6 family screening
Mutator S Homolog 6 (MSH6) gene analysis for known familial variants to facilitate family member screening in Lynch syndrome.
In Plain Language
Family Lynch syndrome test; Inherited cancer genetic testing
Clinical Context
Targeted MSH6 testing of family members for previously identified variants to improve diagnostic efficiency and cancer surveillance.
RVU Information
CPT 81299 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 81299?
CPT 81299 (Msh6 gene known variants) is a Pathology & Lab code. Mutator S Homolog 6 (MSH6) gene analysis for known familial variants to facilitate family member screening in Lynch syndrome.
Who uses CPT code 81299?
CPT 81299 is used by Pathology, Oncology, Gastroenterology. Targeted MSH6 testing of family members for previously identified variants to improve diagnostic efficiency and cancer surveillance.
When is CPT 81299 used?
Targeted MSH6 testing of family members for previously identified variants to improve diagnostic efficiency and cancer surveillance.
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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.