rs12716080, CTNND2

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.
Moderate myopia
CUI: C4315867
Disease: Moderate myopia
8 0.882 0.040 5 11166836 intron variant G/T snv 0.39 0.010 1 2011 2011
Myopia
CUI: C0027092
Disease: Myopia
167 0.882 0.040 5 11166836 intron variant G/T snv 0.39 0.010 1.000 1 2014 2014
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 5 11166836 intron variant G/T snv 0.39 0.010 1 2011 2011