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.
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
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
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
586 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 0.833 6 2007 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 1.000 6 2012 2019
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
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
307 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 1.000 6 2010 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
968 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.050 0.800 5 2008 2012
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
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.050 1.000 5 2012 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
635 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.040 0.750 4 2014 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.040 0.750 4 2011 2019
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
448 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.030 1.000 3 2007 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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.030 0.667 3 2010 2019
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
411 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2009 2015
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
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
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
125 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2015 2019
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