Gene entry
RGS9
regulator of G protein signaling 9
- Chromosome
- 17
- Cytoband
- 17q24.1
- Variants (rsID)
- 22
RGS9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q24.1). Its official name is “regulator of G protein signaling 9”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs34797451Benignsingle nucleotide variant
- rs121908449Pathogenicsingle nucleotide variantBradyopsia|Leber congenital amaurosis
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.