rs104893768, RHO

N. diseases: 3
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.
Retinitis Pigmentosa 4
CUI: C3151001
Disease: Retinitis Pigmentosa 4
36 0.807 0.080 3 129528801 missense variant C/A snv 0.800 1.000 0 1990 2009
Fundus Albipunctatus
CUI: C0311338
Disease: Fundus Albipunctatus
9 0.807 0.080 3 129528801 missense variant C/A snv 0.700 0
Night Blindness, Congenital Stationary, Autosomal Dominant 1
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
5 0.807 0.080 3 129528801 missense variant C/A snv 0.700 0