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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.280 | 6 | 31168676 | intron variant | A/G | snv | 0.78 |
|
0.820 | 0.750 | 1 | 2014 | 2017 | ||||||||
|
0.851 | 0.280 | 6 | 32658495 | upstream gene variant | C/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv |
|
0.900 | 0.966 | 5 | 2007 | 2019 | |||||||||
|
0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 |
|
0.840 | 1.000 | 4 | 2008 | 2017 | |||||||
|
0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 |
|
0.800 | 1.000 | 2 | 2012 | 2014 | ||||||||
|
0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv |
|
0.710 | 1.000 | 1 | 2012 | 2016 | |||||||||
|
0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv |
|
0.900 | 0.889 | 1 | 2008 | 2019 | |||||||||
|
0.807 | 0.200 | 6 | 20661019 | intron variant | G/A;C;T | snv |
|
0.900 | 0.958 | 8 | 2007 | 2019 | |||||||||
|
0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv |
|
0.880 | 1.000 | 4 | 2009 | 2019 | |||||||||
|
0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 |
|
0.880 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.882 | 0.200 | 10 | 69171718 | 3 prime UTR variant | C/T | snv | 0.22 |
|
0.800 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.827 | 0.200 | 12 | 71269322 | intron variant | C/T | snv | 0.75 |
|
0.840 | 1.000 | 2 | 2008 | 2017 | ||||||||
|
0.851 | 0.200 | 9 | 4293150 | intron variant | A/C | snv | 0.57 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.200 | 17 | 37743574 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.200 | 17 | 37742390 | intron variant | G/A | snv | 0.50 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv |
|
0.710 | 1.000 | 1 | 2012 | 2013 | |||||||||
|
0.882 | 0.200 | 6 | 32717773 | upstream gene variant | G/A | snv | 8.5E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.200 | 1 | 205945629 | upstream gene variant | A/G | snv | 0.36 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.200 | 1 | 205930467 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.160 | 3 | 185811292 | intron variant | A/C | snv | 0.46 |
|
0.900 | 0.963 | 9 | 2007 | 2017 | ||||||||
|
0.827 | 0.160 | 11 | 17387083 | missense variant | C/T | snv | 0.64 | 0.71 |
|
0.860 | 0.941 | 8 | 2007 | 2018 | |||||||
|
0.851 | 0.160 | 10 | 112994329 | intron variant | T/C | snv | 0.34 |
|
0.900 | 1.000 | 4 | 2006 | 2020 |