Gene: OPN1MW ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894914
rs104894914
OPN1MW
0.800 GeneticVariation UNIPROT Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies. 12051694

2002
dbSNP: rs104894915
rs104894915
OPN1MW
0.800 GeneticVariation UNIPROT Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies. 12051694

2002
dbSNP: rs104894916
rs104894916
OPN1MW
0.800 GeneticVariation UNIPROT Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies. 12051694

2002
dbSNP: rs104894914
rs104894914
OPN1MW
0.800 GeneticVariation UNIPROT Defective colour vision associated with a missense mutation in the human green visual pigment gene. 1302020

1992
dbSNP: rs104894915
rs104894915
OPN1MW
0.800 GeneticVariation UNIPROT Defective colour vision associated with a missense mutation in the human green visual pigment gene. 1302020

1992
dbSNP: rs104894916
rs104894916
OPN1MW
0.800 GeneticVariation UNIPROT Defective colour vision associated with a missense mutation in the human green visual pigment gene. 1302020

1992
dbSNP: rs104894914
rs104894914
OPN1MW
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894915
rs104894915
OPN1MW
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894916
rs104894916
OPN1MW
A 0.800 CausalMutation CLINVAR

dbSNP: rs724159983
rs724159983
OPN1MW
C 0.700 CausalMutation CLINVAR