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
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)
1 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.700 0
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2017 2017
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2010 2010
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2015 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 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
824 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2002 2002
Hemorrhagic Fever, Crimean
CUI: C0019099
Disease: Hemorrhagic Fever, Crimean
9 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2019 2019
Macroangiopathy
CUI: C1096293
Disease: Macroangiopathy
6 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2018 2018
Polyendocrinopathies, Autoimmune
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
21 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2017 2017
Post MI
CUI: C0856742
Disease: Post MI
4 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2011 2011
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2002 2002
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2014 2014
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.020 0.500 2 2001 2004
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
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
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
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
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
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 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