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
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
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
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
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
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
46 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2006 2006
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
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
112 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2007 2007
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2007 2007
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2007 2007
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
321 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2008 2008
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
109 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2008 2008
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
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
51 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
256 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1 2010 2010
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
85 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
412 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
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