rs13382811, ZEB2

N. diseases: 4
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, Degenerative
CUI: C0154778
Disease: Myopia, Degenerative
58 0.882 0.040 2 144466053 intron variant C/T snv 0.21 0.700 1.000 1 2013 2013
Myopia
CUI: C0027092
Disease: Myopia
167 0.882 0.040 2 144466053 intron variant C/T snv 0.21 0.020 0.500 2 2017 2019
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 2 144466053 intron variant C/T snv 0.21 0.020 1.000 2 2017 2019
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.882 0.040 2 144466053 intron variant C/T snv 0.21 0.010 1.000 1 2019 2019