rs2233789, RDH8

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Myopia
CUI: C0027092
Disease: Myopia
167 0.925 0.040 19 10013026 upstream gene variant C/A;T snv 0.010 1.000 1 2010 2010
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.925 0.040 19 10013026 upstream gene variant C/A;T snv 0.010 1 2010 2010