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 | 2 | 240775895 | missense variant | G/A | snv | 0.700 | 0 | |||||||||
|
1 | 1.000 | 2 | 240783075 | missense variant | A/G | snv | 0.700 | 0 | |||||||||
|
1 | 1.000 | 2 | 240758372 | missense variant | C/T | snv | 4.1E-06 | 1.4E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 2 | 240763217 | missense variant | C/T | snv | 0.700 | 0 | |||||||||
|
3 | 0.882 | 0.080 | 2 | 240783788 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 240740133 | stop gained | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 2 | 240775890 | stop gained | G/A;C | snv | 7.0E-06 | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 240763087 | stop gained | G/A | snv | 4.5E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 2 | 240788191 | missense variant | G/A | snv | 6.4E-05 | 4.2E-05 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.080 | 2 | 240783087 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 2 | 240788149 | missense variant | A/C | snv | 0.700 | 0 | |||||||||
|
5 | 0.851 | 0.120 | 2 | 240783777 | missense variant | G/A | snv | 0.700 | 0 |