rs9982601, None

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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.080 21 34226827 intron variant C/T snv 0.15 0.820 1.000 3 2009 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.080 21 34226827 intron variant C/T snv 0.15 0.810 1.000 4 2011 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.080 21 34226827 intron variant C/T snv 0.15 0.700 1.000 2 2013 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.851 0.080 21 34226827 intron variant C/T snv 0.15 0.700 1.000 1 2013 2013