rs7744813, KCNQ5

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 0.925 0.040 6 72933566 intron variant C/A snv 0.66 0.710 1.000 2 2016 2017
Abnormality of refraction
CUI: C4025843
Disease: Abnormality of refraction
31 0.925 0.040 6 72933566 intron variant C/A snv 0.66 0.700 1.000 1 2013 2013
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.925 0.040 6 72933566 intron variant C/A snv 0.66 0.700 1.000 1 2013 2013