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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Breast Carcinoma
|
2793 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.050 | 0.800 | 5 | 2010 | 2018 | ||||||
Malignant neoplasm of breast
|
3417 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.050 | 0.800 | 5 | 2010 | 2018 | ||||||
Malignant neoplasm of prostate
|
1082 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.040 | 0.500 | 4 | 2009 | 2015 | ||||||
Prostate carcinoma
|
1168 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.040 | 0.500 | 4 | 2009 | 2015 | ||||||
Cardiovascular Diseases
|
711 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.030 | 0.667 | 3 | 2006 | 2014 | ||||||
Cerebrovascular accident
|
591 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.030 | 1.000 | 3 | 2011 | 2015 | ||||||
Coronary Artery Disease
|
1577 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.030 | 1.000 | 3 | 2009 | 2014 | ||||||
Ischemic stroke
|
704 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.030 | 0.667 | 3 | 2006 | 2019 | ||||||
Liver carcinoma
|
942 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.030 | 0.667 | 3 | 2011 | 2018 | ||||||
Alzheimer's Disease
|
1843 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2015 | 2016 | ||||||
Carcinoma of lung
|
1204 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2012 | 2015 | ||||||
Colorectal Carcinoma
|
1962 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2013 | ||||||
Coronary Arteriosclerosis
|
440 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2014 | ||||||
Coronary heart disease
|
1178 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2014 | ||||||
Gallbladder Carcinoma
|
75 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||
Malignant neoplasm of gallbladder
|
81 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||
Malignant neoplasm of lung
|
1142 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2012 | 2015 | ||||||
Malignant Neoplasms
|
1641 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2011 | 2013 | ||||||
Myocardial Infarction
|
680 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 0.500 | 2 | 2006 | 2009 | ||||||
Primary malignant neoplasm
|
1374 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2011 | 2013 | ||||||
Primary malignant neoplasm of lung
|
981 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2012 | 2015 | ||||||
Stage 0 Gallbladder Cancer AJCC v8
|
56 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||
Stage IIA Gallbladder Cancer AJCC v8
|
56 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||
Stage IIB Gallbladder Cancer AJCC v8
|
56 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||
Stage III Gallbladder Cancer AJCC v8
|
56 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2011 |