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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 0.710 | 1.000 | 7 | 2013 | 2019 | |||||
|
4 | 0.882 | 0.280 | 1 | 155904496 | missense variant | A/C;G;T | snv | 0.710 | 1.000 | 1 | 2016 | 2016 | |||||
|
16 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 0.700 | 1.000 | 7 | 2013 | 2016 | |||||
|
2 | 0.925 | 0.160 | 1 | 155910658 | missense variant | C/G | snv | 7.0E-06 | 0.700 | 1.000 | 5 | 2013 | 2016 | ||||
|
3 | 0.882 | 0.160 | 1 | 155904456 | missense variant | C/G | snv | 0.700 | 1.000 | 4 | 2013 | 2014 | |||||
|
9 | 0.827 | 0.160 | 1 | 155904739 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 3 | 2014 | 2016 | |||||
|
2 | 0.925 | 0.160 | 1 | 155904498 | missense variant | T/C | snv | 0.700 | 1.000 | 3 | 2013 | 2016 | |||||
|
1 | 1.000 | 0.160 | 1 | 155904489 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
15 | 0.776 | 0.360 | 1 | 155904494 | stop gained | A/C;G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 1 | 155910462 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 1 | 155904499 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
11 | 0.790 | 0.280 | 1 | 155904493 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.160 | 1 | 155904475 | missense variant | A/G | snv | 0.700 | 0 |