81320 Plcg2 gene common variants
Also known as: PLCG2 variant testing, autoinflammatory disease genetic test
Phospholipase C Gamma 2 (PLCG2) gene analysis for common variants associated with autoinflammatory disease and lymphoproliferative disorders.
In Plain Language
Immune system disorder genetic test; Inflammation disorder marker
Clinical Context
Identifies PLCG2 variants causing autoinflammatory lymphoproliferative and immunodeficiency syndrome and related disorders.
RVU Information
CPT 81320 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 81320?
CPT 81320 (Plcg2 gene common variants) is a Pathology & Lab code. Phospholipase C Gamma 2 (PLCG2) gene analysis for common variants associated with autoinflammatory disease and lymphoproliferative disorders.
Who uses CPT code 81320?
CPT 81320 is used by Pathology, Immunology, Genetics. Identifies PLCG2 variants causing autoinflammatory lymphoproliferative and immunodeficiency syndrome and related disorders.
When is CPT 81320 used?
Identifies PLCG2 variants causing autoinflammatory lymphoproliferative and immunodeficiency syndrome and related disorders.
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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.