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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.776 | 0.120 | 1 | 55057454 | missense variant | G/A;C;T | snv | 7.2E-05 | 0.100 | 1.000 | 11 | 2004 | 2020 | ||||
|
7 | 0.807 | 0.120 | 1 | 55044016 | missense variant | T/A | snv | 0.030 | 1.000 | 3 | 2007 | 2009 | |||||
|
28 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 0.020 | 0.500 | 2 | 2015 | 2018 | ||||
|
3 | 0.882 | 0.080 | 1 | 55058549 | missense variant | C/T | snv | 6.0E-04 | 2.8E-03 | 0.010 | 1.000 | 1 | 2005 | 2005 | |||
|
2 | 0.925 | 0.040 | 1 | 55052407 | frameshift variant | -/T | ins | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
3 | 0.882 | 0.040 | 1 | 55057404 | missense variant | G/A;T | snv | 4.0E-05; 1.2E-05 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
9 | 0.776 | 0.160 | 1 | 55058630 | missense variant | C/T | snv | 4.4E-05 | 2.8E-05 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
18 | 0.732 | 0.360 | 1 | 55063514 | missense variant | G/A | snv | 0.95 | 0.90 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
8 | 0.827 | 0.280 | 1 | 55058564 | missense variant | G/A | snv | 0.86 | 0.83 | 0.010 | < 0.001 | 1 | 2015 | 2015 | |||
|
6 | 0.807 | 0.160 | 1 | 55039931 | missense variant | G/A | snv | 2.8E-05 | 2.8E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
3 | 0.882 | 0.080 | 1 | 55052398 | missense variant | G/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
3 | 0.882 | 0.040 | 1 | 55052408 | missense variant | A/T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 |