OPN1MW, opsin 1, medium wave sensitive, 2652

N. diseases: 107; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894914
rs104894914
0.851 0.120 X 154191716 missense variant T/C snv
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.800 1.000 2 1992 2002
dbSNP: rs104894915
rs104894915
1.000 0.120 X 154187939 missense variant C/A snv
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.800 1.000 2 1992 2002
dbSNP: rs104894916
rs104894916
1.000 0.120 X 154195934 missense variant G/A snv
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.800 1.000 2 1992 2002
dbSNP: rs724159983
rs724159983
1.000 0.120 X 154182566 upstream gene variant A/C snv
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.700 0