| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 155142784 | upstream gene variant | T/C | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 15502209 | intron variant | T/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.120 | 1 | 150977586 | upstream gene variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 1 | 155183255 | intron variant | G/A | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1 | 186749129 | intergenic variant | C/T | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 48071126 | intron variant | A/G | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 91065465 | intergenic variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 145709649 | upstream gene variant | G/A | snv | 3.3E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 93388629 | upstream gene variant | C/G | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 156091431 | intron variant | G/C;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.925 | 0.120 | 1 | 35015950 | intron variant | T/C | snv | 6.2E-03 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1 | 26958422 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.925 | 0.120 | 1 | 145698627 | intron variant | A/G | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 6 | 2009 | 2019 | |||||||
|
0.882 | 0.120 | 2 | 120548864 | upstream gene variant | G/A | snv | 0.33 |
|
0.700 | 1.000 | 3 | 2013 | 2019 | ||||||||
|
0.925 | 0.120 | 2 | 147958859 | missense variant | T/A;C;G | snv | 0.36; 8.4E-06 |
|
0.700 | 1.000 | 3 | 2013 | 2019 | ||||||||
|
2 | 169343942 | intron variant | A/T | snv | 4.6E-02 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
2 | 169154948 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 2 | 2018 | 2019 | |||||||||||
|
2 | 169348613 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||||
|
0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 |
|
0.800 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 |
|
0.800 | 1.000 | 2 | 2009 | 2015 | ||||||||
|
2 | 37023748 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
2 | 9106592 | upstream gene variant | T/C | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 653623 | intergenic variant | C/G | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |