| 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 | 7 | 114802983 | intergenic variant | G/A | snv | 0.44 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 3 | 17813106 | intron variant | A/G | snv | 1.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 18 | 8168062 | intron variant | T/C | snv | 1.9E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 9 | 17993591 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 8 | 38737138 | intron variant | C/T | snv | 0.39 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
13 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 18 | 4414795 | intron variant | A/C | snv | 6.7E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 19 | 41015627 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 11 | 5824251 | intron variant | G/A | snv | 6.9E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 18 | 46590193 | intron variant | T/C | snv | 7.3E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 12 | 12643133 | 3 prime UTR variant | G/T | snv | 1.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 3 | 180064474 | intergenic variant | T/C | snv | 9.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 16 | 73126071 | intron variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 2 | 30503825 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2017 | 2017 |