Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Nervous System Diseases; Mental Disorders | 0.020 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2009 | 2014 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
0.020 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
0.020 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2009 | 2014 | ||||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.020 | 0.500 | 2 | 2006 | 2009 | ||||||||
|
0.851 | 0.160 | 1 | 186676795 | intron variant | C/T | snv | 0.14 | 0.19 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2010 | 2015 | ||||||
|
0.851 | 0.160 | 1 | 186676795 | intron variant | C/T | snv | 0.14 | 0.19 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2010 | 2015 | ||||||
|
0.851 | 0.160 | 1 | 186676795 | intron variant | C/T | snv | 0.14 | 0.19 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2010 | 2015 | ||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms; Male Urogenital Diseases | 0.020 | 0.500 | 2 | 2008 | 2011 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms; Male Urogenital Diseases | 0.020 | 0.500 | 2 | 2008 | 2011 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2013 | 2013 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.790 | 0.160 | 1 | 186679065 | synonymous variant | C/G;T | snv | 0.12; 8.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.020 | 1.000 | 2 | 2012 | 2015 | |||||||
|
0.637 | 0.640 | 1 | 186681619 | upstream gene variant | T/C | snv | 0.17 |
|
Neoplasms | 0.020 | 0.500 | 2 | 2015 | 2016 | |||||||
|
0.637 | 0.640 | 1 | 186681619 | upstream gene variant | T/C | snv | 0.17 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2016 |