rs7493, PON2

N. diseases: 24
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 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.070 0.857 7 2000 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.060 0.667 6 1998 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.030 1.000 3 2002 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.030 1.000 3 2007 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.020 1.000 2 2008 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.020 0.500 2 2008 2010
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.020 0.500 2 2008 2010
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.020 1.000 2 2009 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.020 1.000 2 2004 2007
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2009 2009
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2004 2004
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2007 2007
Chronic glomerulonephritis
CUI: C0152451
Disease: Chronic glomerulonephritis
7 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2014 2014
Dementia
CUI: C0497327
Disease: Dementia
176 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2002 2002
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2002 2002
First myocardial infarction
CUI: C1273976
Disease: First myocardial infarction
7 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2010 2010
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2010 2010
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2006 2006
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2006 2006
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2019 2019
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2006 2006
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1 2002 2002
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2012 2012