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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.160 | 12 | 112477882 | missense variant | A/G | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.160 | 2 | 39007033 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.160 | 7 | 140777995 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.160 | 12 | 112450508 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140801531 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12608823 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12604204 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140781599 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140801533 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140801487 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140801479 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 38996981 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.160 | 2 | 39058683 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.160 | 2 | 39054822 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12608895 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12591729 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140734763 | missense variant | G/A;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12611985 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140778059 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 19 | 4101105 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 3 | 12585794 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
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 |