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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
Digestive System Diseases; Neoplasms | 0.830 | 1.000 | 3 | 2010 | 2018 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
20 | 62317060 | intron variant | G/A | snv | 0.54 | 0.44 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
20 | 62357369 | intron variant | G/A | snv | 4.3E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
20 | 62322314 | missense variant | C/T | snv | 1.0E-04 | 1.0E-04 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 20 | 62330867 | missense variant | G/A | snv | 4.1E-05 | 8.4E-05 |
|
0.700 | 0 | |||||||||||
|
20 | 62333128 | missense variant | G/T | snv | 1.1E-04 | 5.6E-05 |
|
0.700 | 0 | ||||||||||||
|
20 | 62322722 | missense variant | T/C | snv | 4.3E-05 | 2.9E-05 |
|
0.700 | 0 |