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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
14 | 0.724 | 0.560 | 12 | 25209904 | missense variant | T/A;C | snv | 0.700 | 0 | ||||||||
|
37 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.790 | 0.440 | 10 | 49478437 | stop gained | G/A | snv | 7.2E-05 | 4.9E-05 | 0.700 | 0 | ||||||
|
7 | 0.790 | 0.440 | 10 | 49524073 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 9 | 85020233 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
16 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
7 | 0.807 | 0.280 | 7 | 140749365 | missense variant | A/C;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 11 | 11352722 | missense variant | A/G | snv | 0.48 | 0.41 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 3 | 89472571 | missense variant | C/A;T | snv | 8.0E-06; 1.2E-05 | 0.700 | 0 | |||||||
|
7 | 0.790 | 0.440 | 10 | 49472472 | splice acceptor variant | T/C | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
8 | 0.776 | 0.440 | 10 | 49483504 | stop gained | G/A | snv | 1.6E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
7 | 0.790 | 0.280 | 7 | 140801550 | missense variant | G/A;C;T | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.280 | 7 | 140801551 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.280 | 7 | 140801537 | missense variant | T/A;C;G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.827 | 0.280 | 7 | 140753392 | missense variant | A/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.851 | 0.200 | 22 | 28694073 | missense variant | G/A;C;T | snv | 1.7E-05 | 0.700 | 0 | |||||||
|
6 | 0.807 | 0.280 | 17 | 7675157 | missense variant | G/A | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
9 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.800 | 1.000 | 13 | 2002 | 2014 | ||||
|
22 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 0.750 | 1.000 | 12 | 2002 | 2018 | ||||
|
2 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 0.700 | 1.000 | 9 | 2002 | 2013 | |||||
|
8 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 9 | 2002 | 2013 | ||||
|
1 | 1.000 | 0.080 | 7 | 140781593 | missense variant | T/C | snv | 0.700 | 1.000 | 8 | 2002 | 2013 | |||||
|
34 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.700 | 1.000 | 8 | 2002 | 2013 | ||||
|
7 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2002 | 2002 |