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 | 1.000 | 0.120 | 10 | 121515289 | missense variant | G/C;T | snv | 0.700 | 1.000 | 2 | 2011 | 2014 | |||||
|
13 | 0.708 | 0.640 | 10 | 121515280 | missense variant | T/C | snv | 0.700 | 1.000 | 2 | 2011 | 2014 | |||||
|
18 | 0.617 | 0.600 | 10 | 121520163 | missense variant | G/A;C | snv | 5.6E-05; 4.0E-06 | 0.700 | 1.000 | 2 | 2011 | 2014 | ||||
|
5 | 0.882 | 0.080 | 10 | 121488063 | missense variant | A/T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 0.925 | 0.080 | 10 | 121498525 | missense variant | T/G | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
1 | 10 | 121488005 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1 | 10 | 121515283 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1 | 0.925 | 0.120 | 10 | 121488003 | missense variant | T/A | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
11 | 0.732 | 0.200 | 3 | 41224607 | missense variant | A/C;G;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
17 | 0.683 | 0.360 | 3 | 41224610 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 10 | 121519989 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
14 | 0.701 | 0.200 | 3 | 41224606 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 0.851 | 0.120 | 10 | 121515263 | missense variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2014 | 2014 |