Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Retinal disorders

Gene: OPN1SW

Amber List (moderate evidence)

OPN1SW (opsin 1, short wave sensitive)
EnsemblGeneIds (GRCh38): ENSG00000128617
EnsemblGeneIds (GRCh37): ENSG00000128617
OMIM: 613522, Gene2Phenotype
OPN1SW is in 1 panel

1 review

Ivone Leong (Genomics England Curator)

I don't know

Submitted on behalf of the GMS Eye specialist group. These genes are also from RetNet. There is currently not enough evidence to rate these genes Green, therefore they have been given an Amber rating.
Created: 27 Dec 2019, 9:10 a.m. | Last Modified: 27 Dec 2019, 9:10 a.m.
Panel Version: 2.5


  • RetNet
  • Expert Review Amber
Clinvar variants
Variants in OPN1SW
Panels with this gene

History Filter Activity

27 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

gene: OPN1SW was added gene: OPN1SW was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS Mode of inheritance for gene: OPN1SW was set to