rs854560, PON1

N. diseases: 113
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
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
3 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.700 0
Enzyme activity finding
CUI: C1827841
Disease: Enzyme activity finding
2 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.700 0
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
CUI: C2674665
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
1 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.700 0
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 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
1178 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
2793 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
3417 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
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 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
704 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
1641 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
990 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
363 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
1843 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
267 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
281 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
1172 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
1644 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
663 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
1022 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
680 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
2387 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
485 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
711 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 1.000 2 2000 2007