Gene entry
FCRL3
Fc receptor like 3
- Chromosome
- 1
- Cytoband
- 1q23.1
- Variants (rsID)
- 12
FCRL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q23.1). Its official name is “Fc receptor like 3”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs7522061Not classifiedmissense_variantAutoimmune Disease|Allergic Rhinitis|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Rhinitis|Sensorineural Hearing Loss|Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Sudden Sensorineural Hearing Loss|Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.