Gene entry
RHO
rhodopsin
- Chromosome
- 3
- Cytoband
- 3q22.1
- Variants (rsID)
- 9
RHO is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q22.1). Its official name is “rhodopsin”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs149079952Benignsingle nucleotide variantRetinitis pigmentosa|Congenital stationary night blindness autosomal dominant 1
- rs55941599Benignsingle nucleotide variantRetinitis pigmentosa|Congenital stationary night blindness autosomal dominant 1
- rs138831590Likely benignsingle nucleotide variantCongenital stationary night blindness autosomal dominant 1|Retinitis pigmentosa
- rs104893774Pathogenicsingle nucleotide variantRetinitis pigmentosa 4
- rs104893775Pathogenicsingle nucleotide variantRetinitis pigmentosa 4|Retinitis punctata albescens|Retinitis pigmentosa|Retinal dystrophy
- rs104893788Pathogenicsingle nucleotide variantRetinitis pigmentosa 4
- rs104893791Pathogenicsingle nucleotide variantRetinitis pigmentosa 4, autosomal recessive|Retinitis pigmentosa 4
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.