| 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 | 0.160 | 10 | 121591810 | intron variant | T/C | snv | 0.56 |
|
0.770 | 1.000 | 7 | 2007 | 2017 | ||||||||
|
0.807 | 0.160 | 16 | 52565276 | intron variant | C/T | snv | 0.20 |
|
0.770 | 1.000 | 7 | 2010 | 2020 | ||||||||
|
0.807 | 0.120 | 17 | 54979110 | intron variant | G/A | snv | 0.29 |
|
0.770 | 0.889 | 7 | 2009 | 2017 | ||||||||
|
0.925 | 0.080 | 16 | 52500255 | intron variant | T/C | snv | 0.61 |
|
0.770 | 0.875 | 7 | 2007 | 2019 | ||||||||
|
0.776 | 0.200 | 14 | 68567965 | intron variant | C/T | snv | 0.16 |
|
0.770 | 0.889 | 7 | 2009 | 2016 | ||||||||
|
0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.760 | 1.000 | 6 | 2006 | 2019 | ||||||||
|
0.882 | 0.080 | 6 | 151944320 | missense variant | A/G | snv |
|
0.760 | 1.000 | 6 | 2000 | 2013 | |||||||||
|
0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 |
|
0.750 | 1.000 | 5 | 2011 | 2019 | ||||||||
|
0.827 | 0.080 | 12 | 28002147 | intergenic variant | A/G | snv | 8.9E-02 |
|
0.750 | 1.000 | 5 | 2012 | 2016 | ||||||||
|
0.605 | 0.600 | 17 | 7675088 | missense variant | C/A;T | snv | 4.0E-06 |
|
0.750 | 1.000 | 5 | 2011 | 2018 | ||||||||
|
0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 |
|
0.750 | 0.833 | 5 | 2010 | 2014 | |||||||
|
0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 |
|
0.740 | 1.000 | 4 | 2010 | 2015 | ||||||||
|
0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 |
|
0.740 | 0.800 | 4 | 2013 | 2016 | |||||||
|
0.851 | 0.080 | 12 | 115398717 | regulatory region variant | A/G | snv | 0.43 |
|
0.740 | 1.000 | 4 | 2012 | 2015 | ||||||||
|
0.882 | 0.160 | 6 | 127279485 | intron variant | G/A | snv | 0.73 |
|
0.740 | 0.800 | 4 | 2008 | 2012 | ||||||||
|
0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 |
|
0.740 | 1.000 | 4 | 2011 | 2020 | ||||||||
|
0.776 | 0.280 | 10 | 121577821 | intron variant | A/G | snv | 0.53 |
|
0.740 | 1.000 | 4 | 2009 | 2017 | ||||||||
|
0.882 | 0.160 | 6 | 151592978 | intron variant | G/A | snv | 6.1E-02 |
|
0.740 | 1.000 | 4 | 2013 | 2015 | ||||||||
|
0.807 | 0.160 | 17 | 43104122 | missense variant | C/A;G | snv | 1.2E-05 |
|
0.740 | 0.958 | 4 | 1994 | 2017 | ||||||||
|
0.851 | 0.080 | 9 | 108126198 | regulatory region variant | G/A;T | snv |
|
0.740 | 1.000 | 4 | 2011 | 2016 | |||||||||
|
0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv |
|
0.730 | 1.000 | 3 | 2014 | 2019 | |||||||||
|
0.807 | 0.160 | 8 | 127375606 | intron variant | T/C | snv | 0.41 |
|
0.730 | 1.000 | 3 | 2010 | 2015 | ||||||||
|
0.882 | 0.160 | 5 | 56727256 | intergenic variant | T/C;G | snv | 0.22 |
|
0.730 | 1.000 | 3 | 2009 | 2014 | ||||||||
|
0.882 | 0.120 | 6 | 81483392 | intergenic variant | T/C | snv | 0.19 |
|
0.730 | 1.000 | 3 | 2012 | 2020 | ||||||||
|
0.790 | 0.280 | 16 | 23621362 | stop gained | C/T | snv | 6.0E-05 | 2.1E-05 |
|
0.730 | 1.000 | 3 | 2010 | 2016 |