rs5082, APOA2

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.
Obesity
CUI: C0028754
Disease: Obesity
1111 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.020 1.000 2 2015 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2008 2008
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2008 2008
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2009 2009
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 0.010 1.000 1 2015 2015