rs1558139, CYP4F2

N. diseases: 6
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.020 1.000 2 2018 2019
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.010 1.000 1 2018 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.010 1.000 1 2008 2008
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.010 1.000 1 2018 2018
Optic Neuritis
CUI: C0029134
Disease: Optic Neuritis
4 0.851 0.160 19 15886754 intron variant G/A snv 0.46 0.010 1.000 1 2018 2018