81298 Msh6 gene full seq
Also known as: MSH6 full sequencing, MSH6 complete analysis
Mutator S Homolog 6 (MSH6) gene full gene sequence analysis to identify variants associated with Lynch syndrome.
In Plain Language
Complete Lynch syndrome genetic test; Hereditary cancer screening
Clinical Context
Full MSH6 sequencing for Lynch syndrome diagnosis, particularly in patients with later-onset disease or endometrial cancer predominance.
RVU Information
CPT 81298 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 81298?
CPT 81298 (Msh6 gene full seq) is a Pathology & Lab code. Mutator S Homolog 6 (MSH6) gene full gene sequence analysis to identify variants associated with Lynch syndrome.
Who uses CPT code 81298?
CPT 81298 is used by Pathology, Oncology, Gastroenterology. Full MSH6 sequencing for Lynch syndrome diagnosis, particularly in patients with later-onset disease or endometrial cancer predominance.
When is CPT 81298 used?
Full MSH6 sequencing for Lynch syndrome diagnosis, particularly in patients with later-onset disease or endometrial cancer predominance.
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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.