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 | 0.120 | 11 | 68406769 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 68386525 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 11 | 68357768 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 0.700 | 1.000 | 5 | 2001 | 2008 | |||
|
1 | 1.000 | 0.120 | 11 | 68386367 | stop gained | C/A;T | snv | 4.0E-06; 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 68386600 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.160 | 11 | 68386342 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 11 | 68386510 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
3 | 0.882 | 0.160 | 11 | 68406550 | missense variant | G/A;C;T | snv | 1.2E-05; 1.2E-05; 3.2E-05 | 0.700 | 1.000 | 5 | 2001 | 2008 | ||||
|
1 | 1.000 | 0.120 | 11 | 68363791 | missense variant | C/T | snv | 1.2E-05 | 0.800 | 1.000 | 5 | 2001 | 2008 | ||||
|
1 | 1.000 | 0.120 | 11 | 68448822 | stop gained | C/G;T | snv | 3.7E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 68425202 | missense variant | C/T | snv | 5.6E-05 | 6.3E-05 | 0.700 | 1.000 | 5 | 2001 | 2008 | |||
|
1 | 1.000 | 0.120 | 11 | 68386499 | missense variant | C/A;T | snv | 2.2E-04 | 0.700 | 1.000 | 5 | 2001 | 2008 |