NYX, nyctalopin, 60506

N. diseases: 36; N. variants: 20
Disease: Night blindness, congenital stationary ×
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: rs1555967281
rs1555967281 		1.000 0.080 X 41474443 inframe deletion TCTTCC/- delins
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0