81254 Gjb6 gene com variants
Also known as: GJB6 common variant panel, Connexin 30 variant testing
Molecular analysis of the GJB6 gene to identify common variants associated with non-syndromic hearing loss.
In Plain Language
hearing loss gene test; genetic deafness screening
Clinical Context
Used to detect GJB6 deletions in non-syndromic hearing loss, particularly in individuals without GJB2 mutations.
RVU Information
CPT 81254 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 81254?
CPT 81254 (Gjb6 gene com variants) is a Pathology & Lab code. Molecular analysis of the GJB6 gene to identify common variants associated with non-syndromic hearing loss.
Who uses CPT code 81254?
CPT 81254 is used by Genetics, Otolaryngology, Pathology. Used to detect GJB6 deletions in non-syndromic hearing loss, particularly in individuals without GJB2 mutations.
When is CPT 81254 used?
Used to detect GJB6 deletions in non-syndromic hearing loss, particularly in individuals without GJB2 mutations.
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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.