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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.827 | 0.160 | 1 | 46192168 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 0.700 | 1.000 | 6 | 2004 | 2014 | |||
|
4 | 0.851 | 0.120 | 1 | 46194860 | synonymous variant | G/A | snv | 4.0E-05 | 2.1E-05 | 0.700 | 1.000 | 5 | 2007 | 2017 | |||
|
3 | 0.882 | 0.120 | 1 | 46189539 | missense variant | C/G;T | snv | 8.0E-06; 1.6E-05 | 0.700 | 1.000 | 5 | 2009 | 2014 | ||||
|
5 | 0.827 | 0.160 | 1 | 46192397 | missense variant | G/A | snv | 3.5E-05 | 0.700 | 1.000 | 4 | 2004 | 2012 | ||||
|
4 | 0.851 | 0.120 | 1 | 46189457 | splice donor variant | C/A;G;T | snv | 8.0E-05; 8.0E-06 | 0.700 | 1.000 | 4 | 2004 | 2017 | ||||
|
4 | 0.851 | 0.120 | 1 | 46192097 | splice donor variant | C/A;T | snv | 6.2E-04 | 0.700 | 1.000 | 3 | 2001 | 2013 | ||||
|
3 | 0.882 | 0.120 | 1 | 46189870 | stop gained | C/G;T | snv | 8.0E-06; 4.0E-06 | 0.700 | 1.000 | 2 | 2004 | 2011 | ||||
|
4 | 0.851 | 0.120 | 1 | 46193874 | stop gained | G/A | snv | 7.0E-06 | 0.700 | 1.000 | 2 | 2006 | 2012 | ||||
|
9 | 0.790 | 0.240 | 1 | 46194853 | stop gained | G/A;T | snv | 2.0E-05 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 1 | 46189973 | missense variant | C/T | snv | 1.0E-02 | 9.8E-03 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||
|
2 | 0.925 | 1 | 46192386 | frameshift variant | G/- | delins | 0.700 | 0 | |||||||||
|
3 | 0.882 | 0.120 | 1 | 46189901 | stop gained | G/A;T | snv | 8.0E-06 | 0.700 | 0 |