Gene entry
RAB23
RAB23, member RAS oncogene family
- Chromosome
- 6
- Cytoband
- 6p12.1-p11.2
- Variants (rsID)
- 5
RAB23 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p12.1-p11.2). Its official name is “RAB23, member RAS oncogene family”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs45479896Conflicting interpretationssingle nucleotide variantCarpenter syndrome|RAB23-related Carpenter syndrome
- rs121908171Pathogenicsingle nucleotide variantRAB23-related Carpenter syndrome|Inborn genetic diseases|Carpenter syndrome
- rs182662Uncertain significancesingle nucleotide variantCarpenter syndrome
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.