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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
19 | 0.763 | 0.240 | 17 | 67918802 | missense variant | G/A;C | snv | 1.2E-05 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
58 | 0.701 | 0.520 | 18 | 33740444 | splice donor variant | G/A | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
16 | 0.827 | 0.280 | 17 | 67975841 | missense variant | T/C;G | snv | 4.0E-06 | 7.0E-06 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||
|
4 | 0.925 | 0.080 | 9 | 35801153 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
29 | 0.752 | 0.320 | 22 | 30946373 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
25 | 0.716 | 0.440 | 10 | 121517378 | missense variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
33 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
57 | 0.724 | 0.440 | 5 | 162095551 | missense variant | G/A;C | snv | 0.700 | 0 | ||||||||
|
56 | 0.683 | 0.280 | 8 | 115604339 | stop gained | G/A;T | snv | 0.700 | 0 | ||||||||
|
13 | 0.807 | 0.160 | 17 | 67912720 | frameshift variant | TG/- | delins | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
43 | 0.752 | 0.360 | 2 | 229830831 | frameshift variant | A/- | delins | 0.700 | 0 | ||||||||
|
11 | 0.851 | 0.080 | 7 | 42045460 | frameshift variant | G/- | delins | 0.700 | 0 | ||||||||
|
12 | 0.851 | 0.200 | 17 | 67909751 | splice donor variant | GAAGGACCAAGG/- | del | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
7 | 0.925 | 0.040 | 9 | 35802550 | frameshift variant | C/- | del | 0.700 | 0 |