rs2288904, SLC44A2

N. diseases: 8
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.720 0.750 4 2015 2020
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.700 1.000 1 2013 2013
Transfusion-Related Acute Lung Injury
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
3 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.020 1.000 2 2015 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.010 1.000 1 2016 2016
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 0.010 1.000 1 2016 2016