Gene entry
XIAP
X-linked inhibitor of apoptosis
- Chromosome
- X
- Cytoband
- Xq25
- Variants (rsID)
- 8
XIAP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq25). Its official name is “X-linked inhibitor of apoptosis”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs182340753Benignsingle nucleotide variantX-linked lymphoproliferative disease due to XIAP deficiency
- rs5956583Benignsingle nucleotide variantX-linked lymphoproliferative disease due to XIAP deficiency|Autoinflammatory syndrome
- rs9856Benignsingle nucleotide variantX-linked lymphoproliferative disease due to XIAP deficiency
- rs104894764Pathogenicsingle nucleotide variantX-linked lymphoproliferative disease due to XIAP 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.
