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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
26 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
9 | 0.776 | 0.160 | 5 | 132461855 | non coding transcript exon variant | A/G | snv | 0.45 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 7 | 22769871 | downstream gene variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
6 | 0.807 | 0.120 | 10 | 89002619 | non coding transcript exon variant | G/C;T | snv | 0.50 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 11 | 36322143 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
15 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
3 | 0.882 | 0.120 | 1 | 4389144 | intergenic variant | A/G | snv | 4.3E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
6 | 0.807 | 0.120 | 1 | 154406893 | intron variant | A/C | snv | 7.2E-02 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 7 | 28147725 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
7 | 0.790 | 0.200 | 6 | 32690139 | TF binding site variant | T/C | snv | 6.2E-02 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 10 | 6047878 | intron variant | T/G | snv | 7.2E-02 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.882 | 0.120 | 18 | 48053250 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
6 | 0.807 | 0.120 | 3 | 46212159 | intron variant | C/T | snv | 0.10 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
7 | 0.807 | 0.120 | 21 | 35340290 | intron variant | T/A;G | snv | 0.72 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.882 | 0.120 | 3 | 64258442 | intron variant | T/C | snv | 0.22 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
8 | 0.807 | 0.120 | 13 | 39781776 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
4 | 0.851 | 0.200 | 13 | 43883879 | missense variant | T/C | snv | 0.700 | 0 |