Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2233789
rs2233789
RDH8
0.925 0.040 19 10013026 upstream gene variant C/A;T snv
CUI: C0027092
Disease: Myopia
Myopia 		0.010 1.000 1 2010 2010
dbSNP: rs2233789
rs2233789
RDH8
0.925 0.040 19 10013026 upstream gene variant C/A;T snv
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 < 0.001 1 2010 2010