rs10500355, RBFOX1

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.
Abnormality of refraction
CUI: C4025843
Disease: Abnormality of refraction
31 0.925 0.040 16 7409346 intron variant T/A snv 0.29 0.700 1.000 1 2013 2013
Myopia
CUI: C0027092
Disease: Myopia
167 0.925 0.040 16 7409346 intron variant T/A snv 0.29 0.700 1.000 1 2016 2016
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.925 0.040 16 7409346 intron variant T/A snv 0.29 0.700 1.000 1 2013 2013