Gene entry
RNF168
ring finger protein 168
- Chromosome
- 3
- Cytoband
- 3q29
- Variants (rsID)
- 7
RNF168 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q29). Its official name is “ring finger protein 168”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs114025031Benignsingle nucleotide variant
- rs3796129Benignsingle nucleotide variantRIDDLE 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.