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 | 13 | 50531198 | intron variant | G/A | snv | 0.21 | 0.700 | 1.000 | 3 | 2010 | 2019 | ||||||
|
2 | 13 | 50532652 | intron variant | G/A | snv | 0.21 | 0.700 | 1.000 | 3 | 2013 | 2019 | ||||||
|
2 | 13 | 50537219 | intron variant | T/G | snv | 0.15 | 0.700 | 1.000 | 2 | 2008 | 2019 | ||||||
|
1 | 13 | 50578475 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
3 | 13 | 50532386 | intron variant | A/T | snv | 0.59 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 50576594 | intron variant | A/C | snv | 0.24 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 50728174 | intron variant | G/A | snv | 0.74 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 13 | 50542765 | intron variant | G/T | snv | 0.15 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 13 | 50571933 | intron variant | C/A;T | snv | 3.9E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 50657252 | intron variant | -/C | delins | 1.4E-05 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 50599596 | intron variant | G/C | snv | 0.13 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 50562603 | intron variant | C/T | snv | 0.69 | 0.700 | 1.000 | 1 | 2017 | 2017 |