| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.200 | 2 | 100142823 | intron variant | T/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 |
|
0.810 | 1.000 | 1 | 2008 | 2009 | ||||||||
|
0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv |
|
0.830 | 1.000 | 1 | 2009 | 2015 | |||||||||
|
0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 2 | 102470310 | upstream gene variant | A/C | snv | 0.78 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 2 | 102476054 | intron variant | C/T | snv | 0.54 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 16 | 10870261 | intron variant | G/T | snv | 0.78 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 11 | 111326133 | downstream gene variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 |
|
0.810 | 1.000 | 1 | 2011 | 2015 | ||||||||
|
0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 |
|
0.810 | 1.000 | 2 | 2008 | 2011 | ||||||||
|
0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 |
|
0.700 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
0.716 | 0.400 | 9 | 114790969 | missense variant | T/A;C | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 10 | 117854099 | intergenic variant | T/C | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 11 | 118625403 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.925 | 0.120 | 11 | 118709156 | intron variant | G/A | snv | 0.19 |
|
0.800 | 1.000 | 1 | 2011 | 2012 | ||||||||
|
0.925 | 0.200 | 11 | 118809939 | regulatory region variant | C/A | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 3 | 119404431 | intron variant | G/A | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.200 | 4 | 122117140 | regulatory region variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
0.800 | 1.000 | 2 | 2007 | 2014 | ||||||||
|
1.000 | 0.080 | 4 | 122340375 | intron variant | A/C | snv | 5.1E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |