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: rs7325450
rs7325450
1.000 0.040 13 23892865 intron variant A/G snv 0.39
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7331047
rs7331047
1.000 0.040 13 23893203 intron variant T/C snv 0.40
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 1.000 1 2011 2011