| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.080 | 9 | 6365683 | intergenic variant | A/C | snv | 0.34 |
|
0.050 | 0.800 | 5 | 2007 | 2019 | ||||||||
|
0.882 | 0.080 | 15 | 32733778 | 3 prime UTR variant | C/T | snv | 0.16 |
|
0.730 | 1.000 | 3 | 2008 | 2015 | ||||||||
|
0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 |
|
0.730 | 1.000 | 3 | 2013 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 |
|
0.830 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 |
|
0.830 | 0.667 | 3 | 2010 | 2013 | ||||||||
|
0.790 | 0.080 | 2 | 218290058 | 5 prime UTR variant | G/A | snv | 0.46 |
|
0.730 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.851 | 0.080 | 7 | 55160316 | missense variant | C/A | snv |
|
0.020 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
1.000 | 0.080 | 1 | 221724004 | intron variant | A/C;T | snv |
|
0.020 | 1.000 | 2 | 2014 | 2015 | |||||||||
|
0.776 | 0.080 | 12 | 50761880 | upstream gene variant | C/T | snv | 0.23 |
|
0.820 | 1.000 | 2 | 2010 | 2012 | ||||||||
|
1.000 | 0.080 | 15 | 32712046 | intergenic variant | G/A | snv | 0.47 |
|
0.020 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
0.925 | 0.080 | 11 | 65493967 | upstream gene variant | C/A;T | snv |
|
0.020 | 1.000 | 2 | 2017 | 2018 | |||||||||
|
1.000 | 0.080 | 7 | 87566646 | intron variant | G/A | snv | 0.39 |
|
0.020 | 1.000 | 2 | 2011 | 2012 | ||||||||
|
0.925 | 0.080 | 10 | 133536297 | intron variant | T/C | snv | 0.73 |
|
0.020 | 1.000 | 2 | 2009 | 2012 | ||||||||
|
0.925 | 0.080 | 15 | 74720557 | missense variant | T/C | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2008 | 2010 | ||||||||
|
0.776 | 0.080 | 15 | 32700910 | downstream gene variant | C/T | snv | 0.11 |
|
0.720 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
1.000 | 0.080 | 5 | 135141069 | intron variant | C/A;T | snv |
|
0.020 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
1.000 | 0.080 | 7 | 2250887 | synonymous variant | C/T | snv | 0.18 | 0.16 |
|
0.020 | 1.000 | 2 | 2011 | 2018 | |||||||
|
1.000 | 0.080 | 14 | 54093300 | regulatory region variant | T/C | snv | 0.48 |
|
0.020 | 1.000 | 2 | 2011 | 2017 | ||||||||
|
0.925 | 0.080 | 12 | 47883930 | intron variant | C/T | snv | 0.20 |
|
0.020 | 0.500 | 2 | 2012 | 2014 | ||||||||
|
0.925 | 0.080 | 3 | 41225816 | synonymous variant | G/A | snv | 3.2E-05 | 4.9E-05 |
|
0.020 | 1.000 | 2 | 2008 | 2014 | |||||||
|
1.000 | 0.080 | 18 | 48923195 | intron variant | C/A;G;T | snv |
|
0.020 | 1.000 | 2 | 2014 | 2016 | |||||||||
|
0.776 | 0.080 | 5 | 135163402 | intron variant | C/A | snv | 0.63 |
|
0.820 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 |
|
0.820 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 19 | 33084158 | intron variant | G/A | snv | 0.29 |
|
0.720 | 1.000 | 2 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 3 | 37012090 | missense variant | C/G;T | snv | 1.6E-05 |
|
0.020 | 1.000 | 2 | 2007 | 2015 |