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 | 0.040 | 14 | 55136284 | intron variant | T/G | snv | 0.48 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 14 | 55136343 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 14 | 55145762 | downstream gene variant | C/T | snv | 5.7E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 55142516 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 55143056 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 14 | 55143237 | intron variant | C/A | snv | 0.36 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 55126454 | intron variant | A/C | snv | 0.36 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
14 | 0.732 | 0.320 | 14 | 55138217 | missense variant | C/A;G | snv | 0.35 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
12 | 0.752 | 0.200 | 14 | 55138318 | missense variant | A/C | snv | 4.1E-06; 0.45 | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||
|
1 | 14 | 55140648 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 55144222 | intron variant | C/G | snv | 0.42 | 0.700 | 1.000 | 1 | 2012 | 2012 |