Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
0.700 0
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding
0.700 0
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
0.010 1.000 1 2002 2002
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 < 0.001 1 2002 2002
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
0.010 < 0.001 1 2002 2002
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 < 0.001 1 2002 2002
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
0.020 0.500 2 2001 2004
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.010 1.000 1 2005 2005
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.010 < 0.001 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0079772
Disease: T-Cell Lymphoma
T-Cell Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 1.000 2 2000 2007
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2007 2007
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease
0.010 1.000 1 2007 2007
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD
0.010 1.000 1 2007 2007
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer
0.010 1.000 1 2008 2008
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2008 2008
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura
0.010 1.000 1 2010 2010
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.010 < 0.001 1 2010 2010
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0080178
Disease: Spina Bifida
Spina Bifida
0.010 1.000 1 2010 2010