rs104893789, RHO

N. diseases: 1
Source: CLINVAR ×
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, Autosomal Dominant 1
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
5 0.882 0.080 3 129532711 missense variant C/A snv 0.800 1.000 0 1993 1999