rs104894916, OPN1MW

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
0.800 GeneticVariation UNIPROT Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies. 12051694 2002
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
0.800 GeneticVariation UNIPROT Defective colour vision associated with a missense mutation in the human green visual pigment gene. 1302020 1992
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
0.800 CausalMutation CLINVAR