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 0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 0.700 1.000 1 2018 2018
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 0.010 1.000 1 2018 2018