| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv |
|
0.820 | 1.000 | 2 | 2008 | 2016 | |||||||||
|
0.752 | 0.320 | 6 | 20728500 | intron variant | T/C | snv | 0.78 |
|
0.800 | 1.000 | 2 | 2008 | 2015 | ||||||||
|
0.752 | 0.400 | 1 | 67274409 | upstream gene variant | G/A | snv | 0.30 |
|
0.710 | 1.000 | 1 | 2006 | 2013 | ||||||||
|
0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 |
|
0.800 | 1.000 | 1 | 2010 | 2016 | ||||||||
|
0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.763 | 0.480 | 18 | 12779948 | upstream gene variant | G/T | snv | 0.83 |
|
0.880 | 1.000 | 4 | 2007 | 2016 | ||||||||
|
0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv |
|
0.850 | 1.000 | 2 | 2008 | 2016 | |||||||||
|
0.763 | 0.200 | 9 | 114796423 | intron variant | C/T | snv | 0.73 |
|
0.760 | 1.000 | 2 | 2005 | 2018 | ||||||||
|
0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 |
|
0.800 | 1.000 | 1 | 2010 | 2017 | ||||||||
|
0.763 | 0.200 | 16 | 50710713 | missense variant | C/A;T | snv | 4.0E-06; 0.19 |
|
0.790 | 1.000 | 1 | 2002 | 2014 | ||||||||
|
0.763 | 0.360 | 9 | 136372044 | missense variant | C/A;T | snv | 4.0E-06; 0.41 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.763 | 0.320 | 11 | 64329761 | upstream gene variant | A/G | snv | 0.28 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.763 | 0.320 | 7 | 28140937 | intron variant | T/C | snv | 0.41 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 |
|
0.800 | 1.000 | 1 | 2012 | 2015 | ||||||||
|
0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 |
|
0.860 | 1.000 | 1 | 2006 | 2019 | ||||||||
|
0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 |
|
0.800 | 0.917 | 1 | 2006 | 2017 | |||||||
|
0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 |
|
0.800 | 1.000 | 1 | 2008 | 2016 | ||||||||
|
0.776 | 0.240 | 21 | 33404389 | intron variant | A/G | snv | 0.69 |
|
0.800 | 1.000 | 1 | 2012 | 2017 | ||||||||
|
0.790 | 0.200 | 8 | 128554935 | intron variant | T/C | snv | 0.19 |
|
0.810 | 1.000 | 2 | 2010 | 2019 | ||||||||
|
0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 |
|
0.820 | 0.667 | 1 | 2008 | 2020 | ||||||||
|
0.790 | 0.280 | 1 | 67287825 | intergenic variant | C/T | snv | 0.55 |
|
0.720 | 1.000 | 1 | 2006 | 2019 | ||||||||
|
0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 |
|
0.850 | 0.875 | 1 | 2008 | 2017 | ||||||||
|
0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.240 | 9 | 114804733 | intron variant | C/T | snv | 0.13 |
|
0.720 | 1.000 | 1 | 2005 | 2016 |