Gene entry
RFXAP
regulatory factor X associated protein
- Chromosome
- 13
- Cytoband
- 13q13.3
- Variants (rsID)
- 4
RFXAP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q13.3). Its official name is “regulatory factor X associated protein”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs193240312Benignsingle nucleotide variantMHC class II deficiency
- rs201754085Benignsingle nucleotide variantMHC class II 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.