| 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 | 103874524 | intron variant | T/C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
2 | 103901432 | intron variant | C/T | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
2 | 103962465 | intron variant | T/C | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 104253070 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
9 | 10436921 | intron variant | A/G | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 104513350 | intergenic variant | T/C | snv | 8.0E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
11 | 104549972 | intron variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
5 | 104620815 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
5 | 104628884 | intron variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 104653288 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
10 | 104659211 | intron variant | G/A | snv | 0.40 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104661150 | intron variant | T/C | snv | 0.75 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104739427 | intron variant | T/C | snv | 8.8E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104771425 | intron variant | G/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 104772466 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104794766 | intron variant | G/A | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 104858690 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
10 | 104917583 | intron variant | C/A | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104936223 | upstream gene variant | A/C | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 104955801 | intron variant | T/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 105004435 | intron variant | A/C | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 105004990 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 105129444 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
12 | 105152394 | missense variant | G/A | snv | 0.95 | 0.95 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
4 | 105231827 | intron variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |