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 | 170403362 | intergenic variant | A/C | snv | 0.71 |
|
0.700 | 1.000 | 3 | 2018 | 2019 | ||||||||||
|
8 | 25784248 | intergenic variant | A/C | snv | 0.38 |
|
0.700 | 1.000 | 3 | 2018 | 2019 | ||||||||||
|
4 | 124299553 | intergenic variant | A/C | snv | 0.30 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
7 | 117314731 | intron variant | A/C | snv | 0.43 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
17 | 76215127 | intron variant | A/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 30712576 | intron variant | A/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 33577433 | downstream gene variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 99577110 | intron variant | A/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 32330644 | intron variant | A/C | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
2 | 37647707 | intron variant | A/C | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
20 | 590823 | intergenic variant | A/C | snv | 1.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 42628277 | intergenic variant | A/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 160858218 | intergenic variant | A/C | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 14188819 | intron variant | A/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 27445562 | intron variant | A/C | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 78786588 | intron variant | A/C | snv | 0.61 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 9303534 | intron variant | A/C | snv | 0.80 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
20 | 64060707 | intron variant | A/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
8 | 59351906 | intergenic variant | A/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 119007857 | regulatory region variant | A/C | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 134741666 | intron variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 129622560 | intergenic variant | A/C | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 66357990 | intron variant | A/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 3 | 52502292 | intron variant | A/C | snv | 0.86 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
3 | 50276096 | non coding transcript exon variant | A/C | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 |