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 | 15 | 83899406 | intron variant | T/A | snv | 0.63 | 0.700 | 1.000 | 3 | 2008 | 2019 | ||||||
|
3 | 15 | 83913372 | missense variant | G/A;T | snv | 1.6E-05; 0.61 | 0.700 | 1.000 | 3 | 2009 | 2019 | ||||||
|
2 | 15 | 83911404 | intron variant | G/A | snv | 0.63 | 0.700 | 1.000 | 2 | 2013 | 2019 | ||||||
|
2 | 15 | 83911830 | intron variant | A/C;T | snv | 0.700 | 1.000 | 2 | 2010 | 2019 | |||||||
|
1 | 15 | 83888924 | intron variant | T/G | snv | 0.62 | 0.700 | 1.000 | 2 | 2015 | 2019 | ||||||
|
3 | 15 | 83904289 | intron variant | T/G | snv | 0.63 | 0.700 | 1.000 | 2 | 2010 | 2019 | ||||||
|
1 | 15 | 83916786 | intron variant | -/TAAA | delins | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 15 | 83769541 | intron variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
2 | 15 | 83854003 | intron variant | C/T | snv | 0.32 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1 | 15 | 83920861 | intron variant | T/G | snv | 0.63 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 15 | 83678999 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
4 | 15 | 83845538 | intron variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1 | 15 | 83917711 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 15 | 83670684 | intron variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
2 | 1.000 | 0.040 | 15 | 84037709 | missense variant | C/T | snv | 0.22 | 0.19 | 0.700 | 1.000 | 1 | 2017 | 2017 |