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 Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.120 4 102609955 intron variant A/G snv 0.64 0.010 1.000 1 2016 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.882 0.120 4 102609955 intron variant A/G snv 0.64 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.120 4 102609955 intron variant A/G snv 0.64 0.010 1.000 1 2014 2014
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.882 0.120 4 102609955 intron variant A/G snv 0.64 0.010 1.000 1 2013 2013