| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 46249498 | downstream gene variant | A/G | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
6 | 108606639 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
6 | 32660307 | intron variant | C/T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
9 | 37044391 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
6 | 30360175 | upstream gene variant | A/G | snv | 8.4E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 72278461 | intron variant | G/A | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 34981231 | intron variant | C/T | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 72258898 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 125026867 | missense variant | C/T | snv | 0.15 | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
11 | 66793511 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
5 | 51363954 | intergenic variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 53775211 | intron variant | C/T | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 21531721 | intron variant | A/G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1 | 2234967 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
3 | 85351651 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
5 | 152675675 | intron variant | A/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
2 | 174376754 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1 | 24038041 | upstream gene variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
3 | 18717009 | intron variant | A/T | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
5 | 152566250 | intron variant | C/G | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
5 | 152659861 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1 | 20762979 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
14 | 71359830 | intron variant | T/C | snv | 3.3E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 50198188 | downstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 |