| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.080 | 10 | 99585609 | intergenic variant | C/T | snv | 0.15 |
|
0.810 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 12 | 6276561 | intergenic variant | C/T | snv | 0.84 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.790 | 0.080 | 1 | 183112059 | intron variant | A/C | snv | 0.37 |
|
0.800 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 |
|
0.730 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv |
|
0.700 | 1.000 | 2 | 2005 | 2005 | |||||||||
|
0.790 | 0.080 | 10 | 99529178 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 2 | 2014 | 2016 | |||||||||
|
0.790 | 0.080 | 17 | 897353 | intron variant | T/C | snv | 2.3E-02 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 |
|
0.830 | 1.000 | 2 | 2012 | 2019 | ||||||||
|
0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 |
|
0.800 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
0.776 | 0.080 | 6 | 35601785 | intron variant | A/G | snv | 0.15 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 14 | 58722643 | intron variant | G/A | snv | 0.12 |
|
0.710 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 15 | 32864185 | intron variant | G/A | snv | 0.15 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 20 | 50440951 | intergenic variant | C/T | snv | 0.49 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | MT | 7275 | missense variant | T/C | snv |
|
0.800 | 1.000 | 2 | 2006 | 2009 | |||||||||
|
1.000 | 0.080 | MT | 6277 | missense variant | G/A | snv |
|
0.800 | 1.000 | 2 | 2006 | 2009 | |||||||||
|
0.776 | 0.080 | 11 | 111286111 | 3 prime UTR variant | T/C | snv | 0.72 |
|
0.710 | 1.000 | 2 | 2012 | 2019 | ||||||||
|
0.776 | 0.080 | 14 | 53952388 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||
|
0.790 | 0.080 | 3 | 40883471 | intergenic variant | T/A | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 40873748 | intron variant | A/G | snv | 0.13 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.677 | 0.320 | 11 | 61796827 | 3 prime UTR variant | G/C;T | snv |
|
0.800 | 1.000 | 2 | 2014 | 2019 | |||||||||
|
0.776 | 0.080 | 13 | 73075014 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||
|
0.790 | 0.080 | 10 | 58811675 | intron variant | C/T | snv | 0.53 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.776 | 0.080 | 15 | 32709533 | intergenic variant | T/A | snv | 0.20 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||
|
0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 |
|
0.700 | 1.000 | 2 | 2019 | 2019 |