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 | 2 | 232850301 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 0.700 | 1.000 | 4 | 2008 | 2015 | |||||
|
1 | 2 | 232791080 | missense variant | T/A | snv | 2.8E-05 | 1.4E-05 | 0.700 | 1.000 | 4 | 2008 | 2015 | |||||
|
1 | 2 | 232847513 | missense variant | T/A;C | snv | 7.2E-05; 1.9E-04; 1.9E-05; 4.8E-06 | 3.1E-04 | 0.700 | 0 | ||||||||
|
1 | 2 | 232791426 | missense variant | A/G | snv | 1.0E-04 | 7.7E-05 | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 2 | 232794835 | missense variant | A/C;G | snv | 3.9E-04; 8.0E-06 | 0.700 | 0 | |||||||
|
2 | 1.000 | 0.040 | 2 | 232756289 | missense variant | A/G | snv | 4.3E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
2 | 1.000 | 0.040 | 2 | 232809731 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 2 | 232790817 | missense variant | A/G | snv | 2.3E-04 | 6.3E-05 | 0.700 | 0 | ||||||
|
1 | 2 | 232794882 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||||
|
1 | 2 | 232790803 | missense variant | C/G;T | snv | 1.2E-05; 1.6E-04 | 0.700 | 0 | |||||||||
|
1 | 2 | 232791124 | missense variant | T/A | snv | 5.5E-04 | 4.5E-04 | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.040 | 2 | 232747740 | missense variant | A/G | snv | 2.6E-04 | 3.2E-04 | 0.700 | 0 | ||||||
|
1 | 2 | 232819834 | missense variant | C/G;T | snv | 4.1E-06; 5.3E-05 | 0.700 | 0 |