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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.080 | 3 | 193643005 | stop gained | C/T | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||
|
2 | 0.925 | 0.080 | 3 | 193666331 | missense variant | A/G | snv | 1.2E-05 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 3 | 193643579 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.080 | 8 | 104945792 | intron variant | A/G | snv | 0.45 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
5 | 0.925 | 0.080 | 19 | 29708415 | missense variant | G/A | snv | 8.0E-06 | 2.8E-05 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
2 | 0.925 | 0.080 | 3 | 100728759 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||
|
3 | 0.882 | 0.080 | 5 | 110761543 | missense variant | C/A;T | snv | 2.8E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
4 | 0.925 | 0.080 | 10 | 124402952 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 1 | 29196234 | stop gained | A/C;G | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 1 | 29216612 | frameshift variant | TGAT/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 5 | 110761295 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.080 | 1 | 29200574 | missense variant | G/A | snv | 6.4E-05 | 6.3E-05 | 0.700 | 0 | ||||||
|
6 | 0.851 | 0.080 | 2 | 240788109 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.080 | 2 | 240785066 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.080 | 2 | 240783791 | missense variant | A/T | snv | 0.700 | 0 | ||||||||
|
3 | 1.000 | 0.080 | 16 | 574693 | stop gained | C/T | snv | 2.1E-05 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.080 | 1 | 29196235 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
3 | 0.882 | 0.080 | 1 | 29202004 | missense variant | C/T | snv | 7.2E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
5 | 0.827 | 0.120 | 1 | 12002033 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2006 | 2011 | |||||
|
7 | 0.827 | 0.120 | 1 | 1529299 | missense variant | C/T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 0.925 | 0.120 | 18 | 12351330 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.851 | 0.120 | 13 | 110176912 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.851 | 0.120 | 2 | 240786339 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
10 | 0.790 | 0.120 | 2 | 240783780 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.807 | 0.120 | 1 | 29200513 | splice donor variant | -/A | delins | 1.4E-04 | 6.3E-05 | 0.700 | 0 |