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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 0.800 | 1.000 | 1 | 2012 | 2018 | ||||
|
3 | 15 | 58434545 | intron variant | G/C | snv | 0.73 | 0.800 | 1.000 | 1 | 2010 | 2019 | ||||||
|
5 | 15 | 58450219 | intron variant | G/A | snv | 0.81 | 0.800 | 1.000 | 1 | 2012 | 2018 | ||||||
|
5 | 15 | 58438954 | intron variant | G/A;C;T | snv | 0.800 | 1.000 | 1 | 2012 | 2019 | |||||||
|
5 | 15 | 58438299 | intron variant | C/G;T | snv | 0.800 | 1.000 | 1 | 2012 | 2013 | |||||||
|
3 | 15 | 58450532 | intron variant | T/G | snv | 0.39 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
3 | 15 | 58436945 | intron variant | C/T | snv | 0.37 | 0.33 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
3 | 15 | 58446561 | intron variant | G/A | snv | 0.37 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
3 | 15 | 58447562 | intron variant | G/C | snv | 0.38 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 15 | 58442806 | intron variant | A/G | snv | 0.83 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
4 | 15 | 58439368 | intron variant | A/G | snv | 0.54 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 15 | 58445142 | intron variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
3 | 15 | 58444579 | intron variant | C/T | snv | 0.39 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 15 | 58448978 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
5 | 15 | 58448935 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
4 | 15 | 58449185 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
3 | 15 | 58451510 | intron variant | C/T | snv | 0.41 | 0.700 | 1.000 | 1 | 2012 | 2012 |