rs2108622, CYP4F2

N. diseases: 20
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.
Vitamin E Assay
CUI: C1142098
Disease: Vitamin E Assay
4 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.800 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.700 1.000 1 2013 2013
Vitamin K Assay
CUI: C0042879
Disease: Vitamin K Assay
6 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.700 1.000 1 2014 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.060 1.000 6 2008 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.050 1.000 5 2012 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.020 1.000 2 2018 2018
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2016 2016
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2008 2008
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2012 2012
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2014 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2019 2019
Drug usage
CUI: C0242510
Disease: Drug usage
21 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2017 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1 2012 2012
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2009 2009
Post transplant diabetes mellitus
CUI: C1504532
Disease: Post transplant diabetes mellitus
11 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.010 1 2012 2012