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: rs6504218
rs6504218
PECAM1
1.000 0.040 17 64330939 intron variant A/G snv 0.55
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2011
dbSNP: rs7225219
rs7225219
PECAM1
17 64330199 intron variant T/A snv 0.75
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs9892152
rs9892152
PECAM1
1.000 0.040 17 64324605 intron variant T/C snv 0.49
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
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: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.040 1.000 4 2003 2016
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: 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: 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: rs668
rs668
PECAM1
0.851 0.240 17 64377836 missense variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.020 1.000 2 2013 2016
dbSNP: rs1011102664
rs1011102664
PECAM1
1.000 0.120 17 64375191 missense variant C/T snv 7.0E-06
CUI: C0038505
Disease: Sturge-Weber Syndrome
Sturge-Weber Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs1011102664
rs1011102664
PECAM1
1.000 0.120 17 64375191 missense variant C/T snv 7.0E-06
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		0.010 1.000 1 2017 2017
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.010 1.000 1 2015 2015
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0867389
Disease: Chronic graft-versus-host disease
Chronic graft-versus-host disease 		0.010 1.000 1 2013 2013
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2014 2014
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: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2009 2009
dbSNP: rs1131012
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2014 2014
dbSNP: rs1186206565
rs1186206565
PECAM1
17 64352432 missense variant C/T snv
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.010 1.000 1 2012 2012
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: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2004 2004