| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv |
|
0.810 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 |
|
0.810 | 1.000 | 1 | 2011 | 2014 | ||||||||
|
0.851 | 0.040 | 14 | 60606157 | upstream gene variant | T/C | snv | 0.45 |
|
0.800 | 1.000 | 4 | 2012 | 2016 | ||||||||
|
0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 |
|
0.800 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.882 | 0.040 | 7 | 116522675 | upstream gene variant | G/A | snv | 0.28 |
|
0.800 | 1.000 | 2 | 2010 | 2014 | ||||||||
|
1.000 | 0.040 | 9 | 22049657 | intron variant | G/A | snv | 0.59 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.925 | 0.040 | 9 | 22040766 | intron variant | C/T | snv | 0.71 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.882 | 0.080 | 8 | 104945792 | intron variant | A/G | snv | 0.45 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 14 | 60331291 | TF binding site variant | T/A;G | snv |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.040 | 2 | 133605461 | regulatory region variant | T/A;C;G | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.040 | 9 | 22056360 | non coding transcript exon variant | A/G | snv | 0.71 |
|
0.800 | 1.000 | 1 | 2012 | 2016 | ||||||||
|
1.000 | 0.040 | 9 | 22050899 | intron variant | A/G | snv | 0.78 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.882 | 0.120 | 9 | 22051671 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.040 | 1 | 91611540 | TF binding site variant | G/A | snv | 0.81 |
|
0.710 | 1.000 | 1 | 2015 | 2018 | ||||||||
|
0.827 | 0.040 | 1 | 165717968 | TF binding site variant | G/A | snv | 0.85 |
|
0.710 | 1.000 | 1 | 2011 | 2014 | ||||||||
|
0.851 | 0.040 | 9 | 104933567 | downstream gene variant | G/A | snv | 0.61 |
|
0.700 | 1.000 | 2 | 2014 | 2018 | ||||||||
|
0.925 | 0.040 | 6 | 1548134 | intergenic variant | A/G | snv | 0.31 |
|
0.700 | 1.000 | 2 | 2016 | 2018 | ||||||||
|
1.000 | 0.040 | 11 | 47323549 | intron variant | T/C | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 3 | 25532695 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 6 | 1922673 | intron variant | G/A | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.040 | 12 | 83644699 | intergenic variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.040 | 14 | 60380283 | intergenic variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1.000 | 0.040 | 11 | 65457848 | intron variant | C/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 1 | 102806868 | intron variant | T/C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 |