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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.860 | 1.000 | 7 | 2010 | 2015 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.810 | 1.000 | 3 | 2009 | 2019 | |||||||
|
0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 |
|
Neoplasms | 0.810 | 1.000 | 2 | 2009 | 2014 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Respiratory Tract Diseases | 0.800 | 1.000 | 17 | 2008 | 2018 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Respiratory Tract Diseases | 0.800 | 1.000 | 16 | 2008 | 2018 | |||||||
|
0.776 | 0.280 | 5 | 1344343 | splice region variant | G/A;T | snv | 0.37; 8.0E-06 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.800 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 |
|
Neoplasms; Respiratory Tract Diseases | 0.750 | 1.000 | 7 | 2008 | 2014 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.740 | 1.000 | 7 | 2010 | 2018 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.740 | 1.000 | 6 | 2009 | 2017 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.740 | 1.000 | 5 | 2010 | 2015 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Respiratory Tract Diseases | 0.730 | 0.750 | 4 | 2013 | 2019 | |||||||
|
0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.720 | 1.000 | 3 | 2010 | 2017 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.720 | 1.000 | 3 | 2010 | 2016 | |||||||
|
0.776 | 0.200 | 5 | 1320132 | intron variant | G/A | snv | 0.47 |
|
Neoplasms; Respiratory Tract Diseases | 0.710 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.710 | 0.667 | 3 | 2010 | 2014 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.710 | 0.667 | 3 | 2010 | 2014 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.700 | 1.000 | 3 | 2009 | 2015 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.700 | 1.000 | 3 | 2009 | 2015 | |||||||
|
0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 |
|
Neoplasms | 0.700 | 1.000 | 3 | 2009 | 2015 | |||||||
|
0.882 | 0.040 | 5 | 1325475 | non coding transcript exon variant | T/C;G | snv |
|
Neoplasms | 0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||
|
0.882 | 0.040 | 5 | 1325475 | non coding transcript exon variant | T/C;G | snv |
|
Neoplasms | 0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||
|
0.882 | 0.040 | 5 | 1325475 | non coding transcript exon variant | T/C;G | snv |
|
Neoplasms | 0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||
|
0.827 | 0.080 | 5 | 1343679 | intron variant | C/T | snv | 0.14 |
|
Neoplasms; Stomatognathic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.827 | 0.080 | 5 | 1343679 | intron variant | C/T | snv | 0.14 |
|
Neoplasms; Stomatognathic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 |