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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
|
3 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.700 | 0 | ||||||||
Enzyme activity finding
|
2 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.700 | 0 | ||||||||
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
|
1 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.700 | 0 | ||||||||
Coronary Artery Disease
|
1577 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.100 | 1.000 | 12 | 2000 | 2019 | |||||
Coronary heart disease
|
1178 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.100 | 0.909 | 11 | 2002 | 2017 | |||||
Coronary Arteriosclerosis
|
440 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.080 | 1.000 | 8 | 2002 | 2017 | |||||
Breast Carcinoma
|
2793 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.070 | 1.000 | 7 | 2006 | 2019 | |||||
Malignant neoplasm of breast
|
3417 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.070 | 1.000 | 7 | 2006 | 2019 | |||||
Diabetes Mellitus, Non-Insulin-Dependent
|
2672 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.060 | 0.833 | 6 | 1999 | 2018 | |||||
Ischemic stroke
|
704 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.060 | 0.833 | 6 | 2007 | 2019 | |||||
Malignant Neoplasms
|
1641 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.060 | 1.000 | 6 | 2012 | 2019 | |||||
Parkinson Disease
|
990 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.060 | 1.000 | 6 | 2004 | 2017 | |||||
Polycystic Ovary Syndrome
|
363 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.060 | 1.000 | 6 | 2010 | 2019 | |||||
Alzheimer's Disease
|
1843 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.050 | 0.800 | 5 | 2008 | 2012 | |||||
Arteriosclerosis
|
267 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.050 | 1.000 | 5 | 2001 | 2019 | |||||
Atherosclerosis
|
281 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.050 | 1.000 | 5 | 2001 | 2019 | |||||
Primary malignant neoplasm
|
1374 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.050 | 1.000 | 5 | 2012 | 2019 | |||||
Lupus Erythematosus, Systemic
|
1172 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.040 | 0.750 | 4 | 2014 | 2019 | |||||
Neoplasms
|
1644 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.040 | 0.750 | 4 | 2011 | 2019 | |||||
Age related macular degeneration
|
663 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.030 | 0.667 | 3 | 2004 | 2013 | |||||
Multiple Sclerosis
|
1022 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.030 | 1.000 | 3 | 2007 | 2013 | |||||
Myocardial Infarction
|
680 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.030 | 1.000 | 3 | 2004 | 2016 | |||||
Rheumatoid Arthritis
|
2387 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.030 | 0.667 | 3 | 2010 | 2019 | |||||
Amyotrophic Lateral Sclerosis
|
485 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.020 | 1.000 | 2 | 2009 | 2015 | |||||
Cardiovascular Diseases
|
711 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 0.020 | 1.000 | 2 | 2000 | 2007 |