OPN1LW, opsin 1, long wave sensitive, 5956

N. diseases: 197; N. variants: 6
Disease: Cone monochromatism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894912
rs104894912
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0339537
Disease:
Cone monochromatism 		T 0.700 CausalMutation CLINVAR