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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.925 | 0.120 | 11 | 103184880 | intron variant | G/A | snv | 8.1E-06 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.120 | 11 | 103257719 | stop gained | C/T | snv | 6.8E-05 | 1.4E-04 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||
|
8 | 1.000 | 0.120 | 11 | 103125293 | stop gained | C/T | snv | 4.5E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103135524 | stop gained | G/A | snv | 1.4E-05 | 0.700 | 0 | |||||||
|
7 | 0.882 | 0.120 | 11 | 103116677 | stop gained | T/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.120 | 11 | 103122879 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103241546 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.882 | 0.120 | 11 | 103120982 | stop gained | G/T | snv | 2.8E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103191520 | stop gained | C/T | snv | 2.2E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.120 | 11 | 103257731 | stop gained | C/T | snv | 1.4E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103173242 | stop gained | C/A;T | snv | 2.1E-05 | 0.700 | 0 | |||||||
|
15 | 0.827 | 0.120 | 11 | 103220720 | missense variant | A/G | snv | 2.4E-04 | 2.6E-04 | 0.700 | 1.000 | 4 | 2009 | 2018 | |||
|
2 | 0.925 | 0.120 | 11 | 103117852 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 0.700 | 1.000 | 3 | 2012 | 2018 | |||
|
1 | 1.000 | 0.120 | 11 | 103199400 | missense variant | T/C | snv | 8.1E-06 | 5.6E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.120 | 11 | 103192150 | missense variant | C/A;T | snv | 5.1E-06; 5.1E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 11 | 103185032 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 11 | 103135630 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103160971 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103163089 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103179047 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103253347 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103479135 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 11 | 103155439 | missense variant | C/A | snv | 1.6E-03 | 1.8E-03 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 11 | 103253341 | missense variant | C/A;T | snv | 3.6E-05; 3.2E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 11 | 103253384 | missense variant | C/T | snv | 3.6E-05; 8.0E-06 | 2.8E-05 | 0.700 | 0 |