OPN1MW, opsin 1, medium wave sensitive, 2652

N. diseases: 107; N. variants: 5
Disease: Cone monochromatism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606927
rs267606927
Entrez Id: 2652
Gene Symbol: OPN1MW
OPN1MW
CUI: C0339537
Disease:
Cone monochromatism 		0.700 GeneticVariation UNIPROT X-linked cone dystrophy caused by mutation of the red and green cone opsins. 20579627 2010