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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2015 2015
Acute periodontitis
CUI: C0001342
Disease: Acute periodontitis
49 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2018 2018
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
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
Aggressive Periodontitis
CUI: C0031106
Disease: Aggressive Periodontitis
59 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2018 2018
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
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
17 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2017 2017
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
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
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2005 2005
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2014 2014
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2015 2015
Bipolar I disorder
CUI: C0853193
Disease: Bipolar I disorder
46 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2012 2012
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2008 2008
Cavernous Hemangioma of Brain
CUI: C2919945
Disease: Cavernous Hemangioma of Brain
43 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2015 2015
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2018 2018
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2012 2012
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
Childhood Renal Cell Carcinoma
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
10 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2011 2011
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
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2016 2016