rs17648524, RBFOX1

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.
Abnormality of refraction
CUI: C4025843
Disease: Abnormality of refraction
31 0.882 0.040 16 7409682 intron variant G/C snv 0.29 0.700 1.000 1 2013 2013
Hyperopia
CUI: C0020490
Disease: Hyperopia
29 0.882 0.040 16 7409682 intron variant G/C snv 0.29 0.700 1.000 1 2014 2014
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.882 0.040 16 7409682 intron variant G/C snv 0.29 0.700 1.000 1 2013 2013
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 16 7409682 intron variant G/C snv 0.29 0.010 1.000 1 2017 2017