rs498186, WTAPP1;MMP1

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.080 11 102798914 intron variant A/C snv 0.40 0.010 1.000 1 2014 2014
Myopia
CUI: C0027092
Disease: Myopia
167 0.925 0.080 11 102798914 intron variant A/C snv 0.40 0.010 1.000 1 2012 2012