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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 13 | 107817853 | intron variant | -/C | ins | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 13 | 107817853 | intron variant | G/C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 13 | 107726915 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 13 | 107725887 | intron variant | C/T | snv | 0.87 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107732899 | intron variant | G/A | snv | 0.84 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107730794 | intron variant | A/G | snv | 0.74 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107722352 | intron variant | C/T | snv | 0.74 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107684525 | intron variant | C/T | snv | 0.86 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107691801 | intron variant | A/G | snv | 0.12 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107734296 | intron variant | G/A | snv | 0.75 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107732933 | intron variant | A/G | snv | 0.79 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107725527 | intron variant | T/C | snv | 0.71 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107684706 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 13 | 107742527 | intron variant | C/T | snv | 0.70 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 13 | 107733026 | intron variant | A/C | snv | 0.74 | 0.700 | 1.000 | 1 | 2013 | 2013 |