rs11572325, 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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.080 1 59896030 intron variant A/T snv 0.12 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.080 1 59896030 intron variant A/T snv 0.12 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.080 1 59896030 intron variant A/T snv 0.12 0.010 1.000 1 2008 2008