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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.