rs514659, ABO

N. diseases: 10
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 0.882 0.120 9 133266790 intron variant C/A;T snv 0.800 1.000 1 2011 2011
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 2 2011 2012
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2011 2011
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2012 2012
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.882 0.120 9 133266790 intron variant C/A;T snv 0.010 1.000 1 2016 2016