rs2280275, CYP2J2

N. diseases: 3
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 0.040 1 59901568 intron variant T/C snv 0.23 0.010 1.000 1 2013 2013
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.040 1 59901568 intron variant T/C snv 0.23 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.040 1 59901568 intron variant T/C snv 0.23 0.010 1.000 1 2019 2019