rs12536657, HGF

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.
Hyperopia
CUI: C0020490
Disease: Hyperopia
29 0.925 0.040 7 81720892 intron variant A/G snv 0.84 0.85 0.020 1.000 2 2010 2019
Moderate myopia
CUI: C4315867
Disease: Moderate myopia
8 0.925 0.040 7 81720892 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2010 2010