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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.882 | 0.120 | 9 | 5078360 | missense variant | A/G | snv | 0.700 | 1.000 | 4 | 2008 | 2012 | |||||
|
1 | 1.000 | 0.120 | 9 | 5078361 | missense variant | G/C | snv | 4.0E-06 | 0.700 | 1.000 | 4 | 2008 | 2012 | ||||
|
2 | 0.925 | 0.120 | 9 | 5078362 | missense variant | A/C;G;T | snv | 0.700 | 1.000 | 4 | 2008 | 2012 | |||||
|
6 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 0.700 | 1.000 | 4 | 2010 | 2012 | |||||
|
9 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 0.700 | 1.000 | 4 | 2009 | 2011 | |||||
|
25 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 0.700 | 1.000 | 3 | 2002 | 2014 | |||||
|
5 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 0.700 | 1.000 | 3 | 2002 | 2014 | |||||
|
1 | 1.000 | 0.120 | 5 | 35873495 | missense variant | A/T | snv | 0.700 | 1.000 | 2 | 2012 | 2012 | |||||
|
6 | 0.807 | 0.240 | 8 | 38414788 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 1.000 | 0.120 | 1 | 64846699 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
5 | 0.851 | 0.120 | 1 | 64846735 | missense variant | G/T | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
16 | 0.742 | 0.520 | 8 | 38414790 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 |