Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.160 | 1 | 40307478 | stop gained | G/A;T | snv | 3.1E-02; 4.0E-06 | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||
|
2 | 0.925 | 0.160 | 1 | 40307451 | missense variant | G/A;C | snv | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||||
|
2 | 0.925 | 0.160 | 1 | 161191082 | 3 prime UTR variant | T/C | snv | 0.12 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 0.925 | 0.160 | 1 | 161191494 | missense variant | G/C | snv | 9.1E-02 | 9.0E-02 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
2 | 0.925 | 0.080 | 10 | 87933228 | stop gained | G/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 10 | 87933094 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 1 | 40307477 | missense variant | T/A;C;G | snv | 0.020 | 0.500 | 2 | 2018 | 2018 | |||||
|
3 | 0.882 | 0.200 | 2 | 112774659 | 3 prime UTR variant | T/C | snv | 0.32 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.925 | 0.160 | 21 | 26953456 | intron variant | C/A;G | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
3 | 0.882 | 0.160 | 21 | 26930036 | missense variant | A/G | snv | 0.83 | 0.89 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
3 | 0.882 | 0.160 | 11 | 102840607 | intron variant | T/C | snv | 0.58 | 0.57 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
4 | 0.882 | 0.160 | 1 | 102888618 | stop gained | G/A | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
4 | 0.851 | 0.200 | 8 | 23201811 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
5 | 0.851 | 0.160 | 1 | 103079209 | intron variant | C/G;T | snv | 0.15 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
5 | 0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
6 | 0.882 | 0.280 | 20 | 62819980 | missense variant | C/T | snv | 4.7E-02 | 4.5E-02 | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||
|
7 | 0.790 | 0.160 | 10 | 87931042 | splice acceptor variant | AGTT/- | delins | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
7 | 0.790 | 0.160 | 10 | 87931094 | splice region variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
7 | 0.790 | 0.160 | 10 | 87933252 | splice donor variant | G/T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
7 | 0.790 | 0.160 | 10 | 87952263 | splice region variant | A/T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
7 | 0.807 | 0.160 | 15 | 65201874 | missense variant | A/G | snv | 0.56 | 0.61 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
7 | 0.790 | 0.160 | 10 | 87952135 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.790 | 0.160 | 10 | 87925557 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
7 | 0.790 | 0.160 | 10 | 87957984 | stop gained | G/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.790 | 0.160 | 10 | 87957872 | stop gained | C/A | snv | 0.700 | 0 |