rs12953, PECAM1

N. diseases: 9
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 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.040 1.000 4 2001 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.020 1.000 2 2004 2005
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2004 2004
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2003 2003
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2003 2003
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2015 2015
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2010 2010
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 0.010 1.000 1 2014 2014