Gene entry
OPN1SW
opsin 1, short wave sensitive
- Chromosome
- 7
- Cytoband
- 7q32.1
- Variants (rsID)
- 10
OPN1SW is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q32.1). Its official name is “opsin 1, short wave sensitive”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs104894032Pathogenicsingle nucleotide variantBlue color blindness
- rs104894033Pathogenicsingle nucleotide variantBlue color blindness
- rs104894031Uncertain significancesingle nucleotide variantBlue color blindness
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.