rs1131012, PECAM1

N. diseases: 10
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 0.280 17 64350416 missense variant T/C snv 0.38 0.040 1.000 4 2001 2013
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2004 2004
Apraxia, Developmental Verbal
CUI: C0750927
Disease: Apraxia, Developmental Verbal
21 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2004 2004
Chronic graft-versus-host disease
CUI: C0867389
Disease: Chronic graft-versus-host disease
17 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2013 2013
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2009 2009
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2004 2004
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2015 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2009 2009
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2014 2014