Gene entry
IRF8
interferon regulatory factor 8
- Chromosome
- 16
- Cytoband
- 16q24.1
- Variants (rsID)
- 14
IRF8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q24.1). Its official name is “interferon regulatory factor 8”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs16939945Benignsingle nucleotide variantImmunodeficiency 32B|Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
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.