rs339501, FGF10

N. diseases: 2
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 5 44365531 intron variant C/T snv 0.94 0.030 1.000 3 2013 2019
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.925 0.040 5 44365531 intron variant C/T snv 0.94 0.030 1.000 3 2013 2019