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 | 1 | 151934697 | regulatory region variant | A/G | snv | 0.29 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
2 | 7 | 113271355 | intergenic variant | A/C;G | snv | 0.25 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
3 | 0.925 | 0.120 | 10 | 59674761 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
7 | 0.882 | 0.200 | 10 | 59709780 | 5 prime UTR variant | T/C | snv | 0.79 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
6 | 0.882 | 0.200 | 10 | 59708831 | intron variant | G/T | snv | 0.79 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
3 | 1.000 | 0.040 | 6 | 110438805 | missense variant | A/G | snv | 0.17 | 0.16 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||
|
2 | 2 | 210195326 | missense variant | T/G | snv | 0.30 | 0.27 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 5 | 132321304 | intron variant | T/C | snv | 0.71 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1 | 5 | 132321007 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1 | 5 | 132403741 | intergenic variant | C/A | snv | 0.72 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1 | 1 | 75670261 | intron variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
4 | 4 | 158709665 | 3 prime UTR variant | T/C | snv | 0.29 | 0.700 | 1.000 | 1 | 2015 | 2015 |