| 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. | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
12 | 0.763 | 0.280 | 17 | 43063930 | missense variant | C/A;G;T | snv | 2.4E-05 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 0.882 | 0.120 | 17 | 43048090 | intron variant | C/T | snv | 2.8E-05 | 0.010 | 1.000 | 1 | 2020 | 2020 | ||||
|
5 | 0.827 | 0.160 | 17 | 43099853 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
9 | 0.790 | 0.200 | 17 | 43093901 | stop gained | G/A | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
6 | 0.827 | 0.200 | 17 | 43092212 | stop gained | C/A | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
8 | 0.790 | 0.200 | 17 | 43092597 | stop gained | A/C;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
9 | 0.763 | 0.200 | 17 | 43094776 | missense variant | C/T | snv | 8.0E-06 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.827 | 0.200 | 17 | 43045773 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
6 | 0.827 | 0.200 | 17 | 43115730 | missense variant | A/C;G;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
5 | 0.827 | 0.200 | 17 | 43092277 | frameshift variant | -/T | delins | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
4 | 0.851 | 0.160 | 17 | 43063333 | splice region variant | C/T | snv | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||
|
3 | 0.882 | 0.120 | 17 | 43094789 | missense variant | T/C;G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2010 | 2010 |