rs854560, PON1

N. diseases: 110
Source: BEFREE ×
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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 0.833 6 1999 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.100 1.000 12 2000 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2000 2007
Microangiopathy, Diabetic
CUI: C0025945
Disease: Microangiopathy, Diabetic
4 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2000 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
266 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.050 1.000 5 2001 2019
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
271 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.050 1.000 5 2001 2019
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
72 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 0.500 2 2001 2004
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.100 0.909 11 2002 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.080 1.000 8 2002 2017
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2002 2011
Diabetes
CUI: C0011847
Disease: Diabetes
611 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2002 2002
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
714 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2002 2002
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
54 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2002 2002
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2002 2002
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 1.000 6 2004 2017
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
390 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.030 0.667 3 2004 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.030 1.000 3 2004 2016
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
217 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2005 2005
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.070 1.000 7 2006 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.070 1.000 7 2006 2019
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2006 2006
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
60 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
193 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006