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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
19 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.700 | 1.000 | 12 | 2005 | 2014 | ||||
|
11 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 11 | 2005 | 2014 | |||||
|
8 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 16 | 2005 | 2015 | |||||
|
15 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 0.700 | 1.000 | 12 | 2005 | 2016 | ||||
|
6 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 9 | 2005 | 2014 | |||||
|
3 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 0.700 | 1.000 | 9 | 2005 | 2014 | |||||
|
5 | 0.742 | 0.320 | 12 | 25245348 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 9 | 2005 | 2014 | |||||
|
6 | 0.807 | 0.240 | 12 | 25225713 | missense variant | T/A;G | snv | 4.0E-06 | 0.700 | 1.000 | 9 | 2005 | 2016 | ||||
|
2 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 8 | 2005 | 2011 | |||||
|
2 | 0.851 | 0.320 | 12 | 25225627 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 1.000 | 8 | 2005 | 2011 | ||||
|
11 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 0.700 | 1.000 | 2 | 2011 | 2014 | |||||
|
1 | 0.882 | 0.160 | 12 | 25245321 | missense variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 |