Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.040 1.000 4 2001 2013
dbSNP: rs12953
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.040 1.000 4 2001 2013
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0024530
Disease: Malaria
Malaria 		0.010 1.000 1 2001 2001
dbSNP: rs1373054855
rs1373054855
PECAM1
1.000 0.120 17 64370017 missense variant A/G snv 1.4E-05
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 < 0.001 1 2002 2002
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 < 0.001 1 2002 2002
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.040 1.000 4 2003 2016
dbSNP: rs1464381306
rs1464381306
PECAM1
1.000 0.040 17 64390632 missense variant A/T snv 1.4E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 1.000 2 2003 2010
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 0.500 2 2003 2005
dbSNP: rs12953
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2003 2003
dbSNP: rs12953
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2003 2003
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2003 2003
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2003 2003
dbSNP: rs12953
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2004 2005
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2004 2005
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis 		0.010 1.000 1 2004 2004
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2004 2004
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0750927
Disease: Apraxia, Developmental Verbal
Apraxia, Developmental Verbal 		0.010 1.000 1 2004 2004
dbSNP: rs12953
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2004 2004
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2004 2004
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2005 2005
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis 		0.010 1.000 1 2005 2005
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia 		0.010 1.000 1 2007 2007
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0860564
Disease: Retinoic acid syndrome
Retinoic acid syndrome 		0.010 1.000 1 2007 2007
dbSNP: rs281865545
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv
CUI: C0002965
Disease: Angina, Unstable
Angina, Unstable 		0.010 1.000 1 2008 2008
dbSNP: rs4072032
rs4072032
PECAM1
1.000 0.040 17 64378896 intron variant G/A snv 0.40
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.010 1.000 1 2008 2008