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: rs1799762
rs1799762
SERPINE1
7 101126425 upstream gene variant -/G delins
CUI: C4016325
Disease: TRANSCRIPTION OF PLASMINOGEN ACTIVATOR INHIBITOR, MODULATOR OF
TRANSCRIPTION OF PLASMINOGEN ACTIVATOR INHIBITOR, MODULATOR OF 		0.700 0
dbSNP: rs1194865614
rs1194865614
SERPINE1
1.000 0.040 7 101132065 splice donor variant -/TA delins 4.0E-06
CUI: C2750067
Disease: Plasminogen Activator Inhibitor-1 Deficiency
Plasminogen Activator Inhibitor-1 Deficiency 		0.700 1.000 1 1992 1992
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 1999 1999
dbSNP: rs1411224107
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2000 2000
dbSNP: rs1411224107
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06
CUI: C0003851
Disease: Arteriosclerosis Obliterans
Arteriosclerosis Obliterans 		0.010 1.000 1 2000 2000
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		0.010 1.000 1 2001 2001
dbSNP: rs1400537035
rs1400537035
SERPINE1
0.882 0.200 7 101131931 missense variant C/A;G;T snv
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		0.010 1.000 1 2002 2002
dbSNP: rs1400537035
rs1400537035
SERPINE1
0.882 0.200 7 101131931 missense variant C/A;G;T snv
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		0.010 1.000 1 2002 2002
dbSNP: rs1400537035
rs1400537035
SERPINE1
0.882 0.200 7 101131931 missense variant C/A;G;T snv
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.010 1.000 1 2002 2002
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		0.010 1.000 1 2003 2003
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2003 2003
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2003 2003
dbSNP: rs1442033697
rs1442033697
SERPINE1
7 101135780 frameshift variant A/- del
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2004 2004
dbSNP: rs532966772
rs532966772
SERPINE1
1.000 0.080 7 101132023 synonymous variant C/T snv 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2006 2006
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome 		0.010 1.000 1 2006 2006
dbSNP: rs769665945
rs769665945
SERPINE1
0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		0.010 < 0.001 1 2006 2006
dbSNP: rs773829498
rs773829498
SERPINE1
0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2006 2006
dbSNP: rs773829498
rs773829498
SERPINE1
0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2006 2006
dbSNP: rs773829498
rs773829498
SERPINE1
0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		0.010 1.000 1 2006 2006
dbSNP: rs1411224107
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06
CUI: C4552766
Disease: Miscarriage
Miscarriage 		0.010 < 0.001 1 2007 2007
dbSNP: rs1411224107
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06
CUI: C0015526
Disease: Factor XII Deficiency
Factor XII Deficiency 		0.010 < 0.001 1 2007 2007
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		0.010 1.000 1 2007 2007
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		0.010 1.000 1 2007 2007
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		0.010 1.000 1 2007 2007
dbSNP: rs1799889
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2008 2008