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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
53 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.807 | 0.320 | 12 | 6944474 | splice acceptor variant | A/G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
30 | 0.752 | 0.480 | 2 | 144399104 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.240 | 18 | 44951954 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
19 | 0.732 | 0.480 | 2 | 174824479 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.200 | 11 | 61766173 | frameshift variant | GCACCGGGCCCCCCATC/T | delins | 0.700 | 0 | ||||||||
|
48 | 0.708 | 0.440 | 16 | 576255 | splice donor variant | G/A;C | snv | 5.7E-05 | 0.700 | 0 | |||||||
|
25 | 0.732 | 0.520 | 20 | 32433408 | stop gained | C/T | snv | 2.0E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
6 | 0.882 | 0.120 | 18 | 22181517 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
19 | 0.790 | 0.200 | 11 | 66211206 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
41 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | ||||||
|
9 | 0.807 | 0.280 | 1 | 240092656 | missense variant | A/C;G;T | snv | 8.0E-06; 4.0E-06 | 0.700 | 0 | |||||||
|
87 | 0.611 | 0.560 | 15 | 23645747 | frameshift variant | G/-;GG | delins | 0.700 | 0 | ||||||||
|
19 | 0.732 | 0.480 | 4 | 6301794 | stop gained | C/T | snv | 6.0E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
5 | 0.882 | 0.400 | 9 | 137728379 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
35 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.160 | 1 | 16044506 | frameshift variant | -/G | delins | 4.3E-06 | 5.6E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.120 | 6 | 10402608 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2012 | 2012 |