Gene entry
RAB39B
RAB39B, member RAS oncogene family
- Chromosome
- X
- Cytoband
- Xq28
- Variants (rsID)
- 1
RAB39B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq28). Its official name is “RAB39B, member RAS oncogene family”. The reference table lists 1 variant (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs17052027Benignsingle nucleotide variantIntellectual disability, X-linked 72
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
