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.
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
Limb ischemia
CUI: C2945695
Disease: Limb ischemia
3 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2005 2005
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2011 2011
PAI-1 4G/5G polymorphism
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
3 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2011 2011
Pulmonary Thromboembolisms
CUI: C0524702
Disease: Pulmonary Thromboembolisms
6 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1 2002 2002
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 2004 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 2011 2014
Lupus anticoagulant disorder
CUI: C0311370
Disease: Lupus anticoagulant disorder
14 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 2005 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 1999 2015
Methylenetetrahydrofolate reductase polymorphism
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
7 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 2009 2009
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.020 0.500 2 1999 2015
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
prothrombin gene mutation
CUI: C1260403
Disease: prothrombin gene mutation
5 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.030 0.667 3 2003 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.040 0.750 4 2000 2009
Prothrombin G20210A mutation
CUI: C2584409
Disease: Prothrombin G20210A mutation
9 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.040 0.750 4 2001 2008
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.090 0.778 9 2001 2013
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
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.100 0.895 19 2000 2015
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.100 0.912 34 1998 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.100 0.947 19 1999 2018
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.100 1.000 13 1999 2016