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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 45179317 | intergenic variant | A/C;T | snv | 0.37 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
8 | 61141904 | intron variant | C/A | snv | 0.23 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
17 | 79823090 | non coding transcript exon variant | G/C | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
14 | 91046685 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||||
|
2 | 132766032 | intron variant | G/A | snv | 0.27 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
17 | 21361084 | regulatory region variant | C/T | snv | 0.49 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
3 | 132039233 | intron variant | G/A | snv | 0.31 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
8 | 63789828 | intron variant | A/T | snv | 0.49 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
5 | 131042334 | intergenic variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
21 | 46628861 | intergenic variant | A/G | snv | 9.3E-03 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
4 | 18510115 | intron variant | A/G | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
19 | 51278201 | intron variant | G/A | snv | 3.4E-02 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
4 | 163438526 | intergenic variant | A/G;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||||
|
8 | 4431055 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||||
|
8 | 137202985 | intergenic variant | G/A | snv | 0.10 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
20 | 40663144 | intergenic variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
21 | 37513203 | 3 prime UTR variant | C/T | snv | 5.5E-02 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
18 | 78982544 | intron variant | G/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
7 | 78200451 | intron variant | G/A | snv | 0.37 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
20 | 1429938 | regulatory region variant | C/T | snv | 0.41 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
5 | 173850244 | regulatory region variant | T/C | snv | 9.0E-03 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
16 | 23793635 | intergenic variant | G/A | snv | 0.16 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
8 | 28164252 | intron variant | G/T | snv | 9.7E-02 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
4 | 3297073 | intron variant | T/C | snv | 0.12 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
19 | 12885926 | missense variant | A/G | snv | 0.37 | 0.36 |
|
0.700 | 1.000 | 2 | 2019 | 2019 |