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 | 0.320 | 17 | 58207906 | missense variant | G/A | snv | 0.700 | 1.000 | 3 | 2006 | 2016 | |||||
|
3 | 0.882 | 0.320 | 17 | 58219175 | frameshift variant | -/CCCGG | delins | 6.6E-06 | 0.700 | 1.000 | 1 | 2006 | 2006 | ||||
|
3 | 0.882 | 0.320 | 17 | 58219149 | splice donor variant | A/G | snv | 0.700 | 1.000 | 1 | 2006 | 2006 | |||||
|
5 | 0.827 | 0.320 | 17 | 58216088 | splice region variant | C/T | snv | 1.3E-04 | 1.3E-04 | 0.700 | 1.000 | 4 | 2007 | 2015 | |||
|
3 | 0.882 | 0.320 | 17 | 58210658 | splice donor variant | C/T | snv | 6.0E-05 | 2.1E-05 | 0.700 | 1.000 | 1 | 2007 | 2007 | |||
|
3 | 0.882 | 0.320 | 17 | 58214740 | splice donor variant | C/T | snv | 1.2E-05 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
4 | 0.851 | 0.320 | 17 | 58206501 | frameshift variant | -/CCTG | delins | 7.2E-05 | 7.0E-06 | 0.700 | 1.000 | 1 | 2007 | 2007 | |||
|
3 | 0.882 | 0.320 | 17 | 58218620 | frameshift variant | AGTTGGC/- | delins | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
2 | 0.925 | 0.320 | 19 | 41354927 | missense variant | T/G | snv | 8.2E-06 | 0.010 | < 0.001 | 1 | 2011 | 2011 | ||||
|
5 | 0.827 | 0.320 | 17 | 58213011 | stop gained | C/A | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
1 | 1.000 | 0.320 | 17 | 58216174 | missense variant | T/C;G | snv | 4.0E-06 | 0.010 | < 0.001 | 1 | 2011 | 2011 | ||||
|
10 | 0.776 | 0.360 | 17 | 58208153 | inframe deletion | GAG/- | delins | 2.0E-05 | 1.4E-05 | 0.700 | 1.000 | 3 | 2014 | 2016 | |||
|
2 | 0.925 | 0.320 | 17 | 58216687 | missense variant | C/A | snv | 0.010 | 1.000 | 1 | 2016 | 2016 |