| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.080 | 9 | 98917470 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.708 | 0.400 | 17 | 7674262 | missense variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.742 | 0.440 | 17 | 7674256 | missense variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.695 | 0.440 | 17 | 7675218 | missense variant | T/C;G | snv | 4.0E-06 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 |
|
0.700 | 1.000 | 4 | 2013 | 2019 | ||||||||
|
0.790 | 0.080 | 20 | 7831703 | downstream gene variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 4 | 2013 | 2019 | ||||||||
|
0.732 | 0.160 | 15 | 32702555 | intergenic variant | T/C | snv | 0.67 |
|
0.700 | 1.000 | 4 | 2008 | 2015 | ||||||||
|
0.716 | 0.160 | 10 | 112520943 | intron variant | T/C | snv | 0.13 |
|
0.700 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 8 | 116611854 | intergenic variant | T/C | snv | 0.19 |
|
0.700 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
19 | 40236313 | missense variant | T/C | snv |
|
0.700 | 1.000 | 2 | 2005 | 2014 | |||||||||||
|
0.790 | 0.080 | 17 | 897353 | intron variant | T/C | snv | 2.3E-02 |
|
0.700 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 11 | 111286111 | 3 prime UTR variant | T/C | snv | 0.72 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 1 | 22261235 | regulatory region variant | T/C | snv | 6.2E-02 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 114402172 | intron variant | T/C | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.776 | 0.200 | 3 | 179234285 | missense variant | T/C | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.776 | 0.080 | 12 | 6297738 | regulatory region variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 9 | 110909123 | intron variant | T/C | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 12 | 50823107 | downstream gene variant | T/C | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 3 | 134029945 | intron variant | T/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.708 | 0.280 | 13 | 32394673 | intron variant | T/C | snv | 6.6E-03 | 6.0E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.776 | 0.080 | 6 | 31042408 | regulatory region variant | T/C | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 2 | 198747683 | intron variant | T/C | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |