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
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
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
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
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
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 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
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
Deficiency of glucose-6-phosphate dehydrogenase
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
20 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2009 2009
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
DiGeorge Syndrome
CUI: C0012236
Disease: DiGeorge Syndrome
7 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2006 2006
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2006 2006
Gastrointestinal adenocarcinoma
CUI: C4552318
Disease: Gastrointestinal adenocarcinoma
3 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2002 2002
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2008 2008
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2006 2006
Homocysteinemia
CUI: C3495426
Disease: Homocysteinemia
6 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
Hypoplasminogenemia
CUI: C0398621
Disease: Hypoplasminogenemia
3 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2000 2000