rs1183194405, F2

N. diseases: 19
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.
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.030 1.000 3 1999 2008
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.020 0.500 2 2002 2008
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.020 1.000 2 2006 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.020 1.000 2 1999 2018
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.020 1.000 2 1999 2007
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2006 2006
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2016 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1 2010 2010
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2011 2011
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2002 2002
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2015 2015
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2005 2005
Inflammatory Bowel Disease 21
CUI: C2676507
Disease: Inflammatory Bowel Disease 21
1 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2002 2002
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2011 2011
Protein C Deficiency
CUI: C0398625
Disease: Protein C Deficiency
14 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 1994 1994
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2019 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2002 2002
Varicose Ulcer
CUI: C0042344
Disease: Varicose Ulcer
2 0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 0.010 1.000 1 2005 2005