Gene: OPN1MW ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2652
Gene Symbol: OPN1MW
OPN1MW 		0.010 GeneticVariation disease BEFREE Rare interchange haplotypes in exon 3 of the OPN1LW and OPN1MW opsin genes cause X-linked myopia, color vision defect, and cone dysfunction. 28358949 2017