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.
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
1 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.700 3 2000 2004
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.050 0.800 5 2000 2007
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.040 0.750 4 2005 2007
Obesity
CUI: C0028754
Disease: Obesity
811 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.030 1.000 3 2001 2007
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.030 0.667 3 2005 2007
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.020 1.000 2 2002 2004
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.020 1.000 2 2002 2004
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.020 1.000 2 2004 2009
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
48 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.020 0.500 2 2004 2007
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1782 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1 2015 2015
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
10 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2004 2004
Heart failure
CUI: C0018801
Disease: Heart failure
91 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2011 2011
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
65 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2011 2011
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
44 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2002 2002
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2004 2004
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
20 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2003 2003
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
26 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2001 2001