rs1799889, SERPINE1

N. diseases: 31
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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.020 1.000 2 2014 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.020 1.000 2 2006 2018
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.020 1.000 2 2018 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.020 1.000 2 2014 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2012 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2018 2018
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2018 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2018 2018
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2012 2012
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2012 2012
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2012 2012
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2013 2013
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2011 2011
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2019 2019
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2013 2013
High altitude pulmonary edema
CUI: C0340100
Disease: High altitude pulmonary edema
45 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2015 2015
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2008 2008
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2011 2011
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2014 2014
Malignant neoplasm of testis
CUI: C0153594
Disease: Malignant neoplasm of testis
31 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2010 2010
Malignant Testicular Germ Cell Tumor
62 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2010 2010
Meningitis, Pneumococcal
CUI: C0025295
Disease: Meningitis, Pneumococcal
13 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2014 2014