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
Diabetes Mellitus, Non-Insulin-Dependent
0.060 0.833 6 1999 2018
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 1.000 12 2000 2019
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: C0025945
Disease: Microangiopathy, Diabetic
Microangiopathy, Diabetic
0.020 1.000 2 2000 2018
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.050 1.000 5 2001 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.050 1.000 5 2001 2019
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: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 0.909 11 2002 2017
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.080 1.000 8 2002 2017
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
0.020 1.000 2 2002 2011
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: 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: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.060 1.000 6 2004 2017
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.030 1.000 3 2004 2016
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.030 0.667 3 2004 2013
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: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.070 1.000 7 2006 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.070 1.000 7 2006 2019
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