Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3 ×
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: rs104893740
rs104893740 		0.925 0.080 3 50193139 missense variant G/A snv 4.0E-06
CUI: C1864870
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.800 1.000 2 1996 2007
dbSNP: rs786205853
rs786205853 		0.925 0.080 3 50194111 missense variant C/G snv
CUI: C1864870
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Autosomal Dominant 3 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.800 0