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 | 0.763 | 0.200 | 15 | 48468097 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48415759 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48432944 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
34 | 0.683 | 0.320 | 15 | 48465820 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
11 | 0.742 | 0.200 | 15 | 48537629 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48495219 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
13 | 0.732 | 0.280 | 15 | 48470705 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.200 | 15 | 48474566 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48515393 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.200 | 15 | 48448894 | splice acceptor variant | C/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.200 | 15 | 48496204 | frameshift variant | GTACACATTCA/- | delins | 0.700 | 0 | ||||||||
|
10 | 0.752 | 0.200 | 15 | 48505037 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48430736 | missense variant | A/G | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.160 | 15 | 48465825 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 15 | 48467975 | missense variant | C/A;G | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 15 | 48467994 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 15 | 48467956 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
10 | 0.752 | 0.200 | 15 | 48515382 | splice region variant | C/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.200 | 15 | 48437898 | stop gained | A/C;T | snv | 0.700 | 0 | ||||||||
|
16 | 0.708 | 0.280 | 15 | 48505106 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
11 | 0.742 | 0.200 | 15 | 48510125 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
10 | 0.752 | 0.200 | 15 | 48495155 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.200 | 15 | 48485374 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48437069 | stop gained | C/A;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.200 | 15 | 48468542 | splice region variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 |