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.
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.020 1.000 2 2014 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.020 1.000 2 2014 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.010 1 2009 2009
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.010 1.000 1 2019 2019
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.010 1.000 1 2018 2018
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.807 0.320 X 12906578 intron variant C/G snv 0.30 0.010 1.000 1 2015 2015