rs644242, PAX6

N. diseases: 3
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 0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 0.030 1.000 3 2011 2018
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 0.020 1.000 2 2012 2014
Cataract
CUI: C0086543
Disease: Cataract
124 0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 0.010 1.000 1 2012 2012