rs1126742, CYP4A11

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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 0.020 1.000 2 2008 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 0.020 1.000 2 2014 2018
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 0.010 1.000 1 2013 2013