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
Night blindness, congenital stationary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2007 2007
dbSNP: rs786205853
rs786205853
0.925 0.080 3 50194111 missense variant C/G snv
Night blindness, congenital stationary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2007 2007