rs662, PON1

N. diseases: 157
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, SUSCEPTIBILITY TO
3 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.700 0
CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
1 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.700 0
Enzyme activity finding
CUI: C1827841
Disease: Enzyme activity finding
2 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.700 0
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 0.864 22 1996 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 1.000 12 1996 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 0.889 27 1998 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 0.938 16 1998 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.100 0.929 14 2000 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.070 1.000 7 2000 2020
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.070 0.857 7 2000 2010
Microangiopathy, Diabetic
CUI: C0025945
Disease: Microangiopathy, Diabetic
4 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 1.000 2 2000 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.060 1.000 6 2001 2019
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.060 1.000 6 2001 2019
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 0.500 2 2001 2018
Coronary Artery Vasospasm
CUI: C0010073
Disease: Coronary Artery Vasospasm
9 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 1.000 2 2002 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1 2002 2002
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.090 0.667 9 2003 2014
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2003 2003
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2003 2003
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.030 0.667 3 2004 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.030 1.000 3 2004 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.020 1.000 2 2004 2015
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2004 2004
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2004 2004
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2004 2004