rs775611802
This variant is located in the OPN1SW gene.
▶ClinVar annotation
Likely Benign★☆☆☆
1 submitter1 publicationAbout OPN1SW
This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]
View all OPN1SW variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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