rs9797861, SLC44A2

N. diseases: 9
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.710 1.000 2 2016 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.710 1.000 2 2016 2016
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
Pulmonary Embolism
CUI: C0034065
Disease: Pulmonary Embolism
16 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016
Transfusion-Related Acute Lung Injury
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
3 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.010 1.000 1 2016 2016