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: 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: 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: 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
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: 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: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.060 0.833 6 2007 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 1.000 6 2012 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.060 1.000 6 2010 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: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 1.000 5 2012 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.050 0.800 5 2008 2012
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: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.040 0.750 4 2014 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.040 0.750 4 2011 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.030 1.000 3 2007 2013
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.030 0.667 3 2010 2019
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: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2008 2019
dbSNP: rs854560
rs854560
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2008 2019