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 | 0.776 | 0.280 | 1 | 11965571 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.160 | 6 | 156829296 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
11 | 0.790 | 0.400 | 12 | 49039277 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
38 | 0.708 | 0.320 | 14 | 92005938 | stop gained | C/A;T | snv | 4.0E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
12 | 0.827 | 0.200 | 19 | 39480879 | stop gained | C/A;G;T | snv | 3.1E-03; 4.6E-06 | 0.700 | 0 | |||||||
|
8 | 0.752 | 0.480 | 17 | 68530405 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.080 | 5 | 140114737 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
5 | 0.925 | 0.080 | 5 | 140114544 | stop gained | C/G;T | snv | 9.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.925 | 0.080 | 5 | 140114964 | stop gained | C/G | snv | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.120 | 16 | 1706450 | stop gained | C/G;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
12 | 0.827 | 0.200 | 19 | 39482885 | stop gained | G/C;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
17 | 0.851 | 0.240 | 17 | 63947062 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
19 | 0.752 | 0.280 | 17 | 63957514 | missense variant | C/T | snv | 8.2E-06 | 1.4E-05 | 0.700 | 1.000 | 2 | 2004 | 2008 | |||
|
58 | 0.677 | 0.360 | 17 | 42687838 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||
|
34 | 0.742 | 0.400 | 16 | 5079077 | missense variant | C/G;T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
46 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
20 | 0.716 | 0.240 | 11 | 2585264 | missense variant | A/G | snv | 4.0E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
13 | 0.851 | 0.360 | 12 | 101642529 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
34 | 0.742 | 0.400 | 16 | 5079078 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
14 | 0.882 | 0.120 | 8 | 22162694 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
10 | 0.807 | 0.200 | 2 | 162273913 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
6 | 0.882 | 0.080 | 5 | 140114470 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
42 | 0.708 | 0.360 | 5 | 140114480 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.080 | 5 | 140114651 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.080 | 5 | 140114446 | missense variant | G/A;C | snv | 0.700 | 0 |