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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 0.790 | 0.120 | 8 | 74364005 | missense variant | C/T | snv | 3.2E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.040 | 2 | 201733377 | missense variant | T/A | snv | 4.9E-04 | 5.9E-04 | 0.700 | 0 | ||||||
|
19 | 0.742 | 0.200 | 2 | 240788118 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.080 | 2 | 240789246 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.851 | 0.080 | 2 | 240788109 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.040 | 2 | 240786513 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.040 | 2 | 240786444 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
6 | 0.851 | 0.120 | 2 | 240786339 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.080 | 2 | 240785066 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
10 | 0.790 | 0.120 | 2 | 240783780 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 2 | 201711091 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
4 | 0.882 | 0.080 | 1 | 11998877 | missense variant | C/T | snv | 8.0E-06 | 0.700 | 0 |