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
760 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.810 1.000 5 2011 2012
Low density lipoprotein cholesterol measurement
676 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.800 8 2008 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.800 4 2009 2015
High density lipoprotein measurement
867 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.800 2 2012 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.800 1 2009 2009
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
52 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2009 2009
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
245 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2017 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2013 2013
Aspartate aminotransferase measurement
108 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2011 2011
Catalase measurement
CUI: C0523550
Disease: Catalase measurement
2 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2017 2017
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.700 1 2012 2012
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
37 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.010 1.000 1 2011 2011
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.010 1.000 1 2014 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
636 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.010 1.000 1 2014 2014
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
41 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 0.010 1.000 1 2014 2014