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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.090 0.889 9 1997 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.070 0.857 7 2001 2009
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.060 1.000 6 1999 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.060 1.000 6 1999 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.050 0.800 5 2003 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.040 0.750 4 1998 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 2009 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 2003 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 2009 2014
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.020 1.000 2 2005 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.020 0.500 2 2003 2007
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.020 0.500 2 2010 2014
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.020 1.000 2 2007 2009
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.020 0.500 2 2010 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2009 2009
Arteriopathic disease
CUI: C0852949
Disease: Arteriopathic disease
14 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2004 2004
Asthma
CUI: C0004096
Disease: Asthma
1536 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2013 2013
Brucellosis
CUI: C0006309
Disease: Brucellosis
30 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2009 2009
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
Endotoxemia
CUI: C0376618
Disease: Endotoxemia
5 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2005 2005
Episodic Kinesigenic Dyskinesia 1
CUI: C4552000
Disease: Episodic Kinesigenic Dyskinesia 1
18 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2020 2020
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1 2013 2013