rs662702, PAX6;ELP4

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 31787522 3 prime UTR variant C/T snv 0.15 0.030 1.000 3 2011 2019
Moderate myopia
CUI: C4315867
Disease: Moderate myopia
8 0.882 0.040 11 31787522 3 prime UTR variant C/T snv 0.15 0.010 1.000 1 2018 2018
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 11 31787522 3 prime UTR variant C/T snv 0.15 0.010 1.000 1 2012 2012