rs6725887, WDR12

N. diseases: 4
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 heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 0.800 1.000 3 2011 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 0.800 1.000 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 0.700 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 0.700 1.000 1 2013 2013