Gene entry
RGR
retinal G protein coupled receptor
- Chromosome
- 10
- Cytoband
- 10q23.1
- Variants (rsID)
- 10
RGR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q23.1). Its official name is “retinal G protein coupled receptor”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs61730895Benignsingle nucleotide variantRetinitis pigmentosa
- rs104894187Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa 44|Cone dystrophy
- rs143720091Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Retinitis pigmentosa 44
- rs143761967Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa
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.