rs104894910, NYX

N. diseases: 3
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.
Night Blindness, Congenital Stationary, Type 1A
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
19 0.882 0.080 X 41473734 missense variant G/C snv 0.700 0
Myopia
CUI: C0027092
Disease: Myopia
167 0.882 0.080 X 41473734 missense variant G/C snv 0.010 1.000 1 2006 2006
Nyctalopia
CUI: C0028077
Disease: Nyctalopia
18 0.882 0.080 X 41473734 missense variant G/C snv 0.010 1.000 1 2006 2006