| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.040 | 8 | 118939661 | intron variant | A/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 11 | 64350711 | intron variant | A/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.882 | 3 | 106229671 | intergenic variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.882 | 5 | 103342219 | intergenic variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.882 | 16 | 11364614 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 |
|
0.810 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
0.900 | 0.980 | 2 | 2005 | 2019 | |||||||
|
0.807 | 0.040 | 19 | 4837475 | upstream gene variant | A/G | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
7 | 37397251 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.882 | 19 | 49693735 | intron variant | A/G | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.882 | 12 | 103493699 | intron variant | A/G | snv | 0.64 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.724 | 0.240 | 12 | 40366829 | non coding transcript exon variant | A/G | snv | 1.7E-02 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.882 | 12 | 94158023 | intron variant | A/G | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.882 | 4 | 10717222 | intergenic variant | A/G | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.724 | 0.240 | 15 | 67171953 | intron variant | A/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.040 | 4 | 26088753 | intron variant | A/G | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.200 | 1 | 167442147 | intron variant | A/G | snv | 0.29 |
|
0.810 | 1.000 | 1 | 2011 | 2013 | ||||||||
|
0.882 | 4 | 40290296 | regulatory region variant | A/G | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1 | 159035859 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
0.882 | 7 | 100698285 | upstream gene variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.851 | 0.040 | 6 | 135581461 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 |