RDH8, retinol dehydrogenase 8, 50700

N. diseases: 6; N. variants: 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: rs1644731
rs1644731
0.925 0.040 19 10021323 missense variant T/A;C snv 4.0E-06; 0.52
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2233789
rs2233789
0.925 0.040 19 10013026 upstream gene variant C/A;T snv
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 < 0.001 1 2010 2010