rs12762303, ALOX5

N. diseases: 4
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 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 0.020 0.500 2 2008 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 0.010 1 2008 2008
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 0.010 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 0.010 1.000 1 2019 2019