rs1188383936, F2

N. diseases: 102
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.
Acquired thrombophilia
CUI: C2585317
Disease: Acquired thrombophilia
2 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2005 2005
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.060 0.833 6 2002 2016
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2006 2006
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.050 1.000 5 1998 2013
Antithrombin III Deficiency
CUI: C0272375
Disease: Antithrombin III Deficiency
52 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 1.000 2 2000 2005
Arterial Occlusive Diseases
CUI: C0003838
Disease: Arterial Occlusive Diseases
4 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 1999 1999
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2008 2008
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.030 0.667 3 2000 2013
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2012 2012
Budd-Chiari Syndrome
CUI: C0856761
Disease: Budd-Chiari Syndrome
4 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 1.000 2 2004 2016
Cardiac Arrest
CUI: C0018790
Disease: Cardiac Arrest
50 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2012 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.030 1.000 3 2011 2019
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2007 2007
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 1.000 2 2000 2009
Cerebral Thrombosis
CUI: C0079102
Disease: Cerebral Thrombosis
7 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2007 2007
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.050 1.000 5 1999 2016
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 1.000 2 2000 2011
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2010 2010
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2011 2011
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 1.000 2 2008 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 2004 2009