rs104894914, OPN1MW

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cone monochromatism
CUI: C0339537
Disease: Cone monochromatism
9 0.851 0.120 X 154191716 missense variant T/C snv 0.810 1.000 2 1995 2012
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
10 0.851 0.120 X 154191716 missense variant T/C snv 0.800 1.000 2 1992 2002
Low Vision
CUI: C0042798
Disease: Low Vision
51 0.851 0.120 X 154191716 missense variant T/C snv 0.010 1.000 1 2014 2014
Nystagmus
CUI: C0028738
Disease: Nystagmus
95 0.851 0.120 X 154191716 missense variant T/C snv 0.010 1.000 1 2014 2014