Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 21028168 | intron variant | T/G | snv | 0.87 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21028168 | intron variant | T/G | snv | 0.87 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21028168 | intron variant | T/G | snv | 0.87 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21037729 | intron variant | G/A | snv | 0.86 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21037729 | intron variant | G/A | snv | 0.86 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21037729 | intron variant | G/A | snv | 0.86 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21040767 | intron variant | T/G | snv | 0.83 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21040767 | intron variant | T/G | snv | 0.83 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21040767 | intron variant | T/G | snv | 0.83 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 3 | 2010 | 2019 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 2 | 2010 | 2019 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.700 | 1.000 | 2 | 2010 | 2012 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |