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 | 0.240 | 1 | 11157174 | missense variant | A/G | snv |
|
0.700 | 1.000 | 4 | 2015 | 2016 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.040 | 1.000 | 4 | 2012 | 2015 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.040 | 1.000 | 4 | 2012 | 2015 | |||||||||
|
0.658 | 0.240 | 1 | 11128107 | missense variant | G/A;T | snv |
|
0.800 | 1.000 | 4 | 2015 | 2016 | |||||||||
|
0.776 | 0.240 | 1 | 11124516 | missense variant | G/A;T | snv |
|
0.800 | 1.000 | 4 | 2015 | 2016 | |||||||||
|
1.000 | 0.080 | 1 | 11139308 | missense variant | C/T | snv | 8.2E-06 | 2.1E-05 |
|
0.700 | 1.000 | 4 | 2015 | 2016 | |||||||
|
1.000 | 1 | 11130648 | missense variant | C/A;T | snv | 8.1E-06; 1.6E-05 |
|
0.700 | 1.000 | 3 | 2015 | 2016 | |||||||||
|
0.925 | 0.160 | 1 | 11129789 | missense variant | A/C | snv |
|
0.800 | 1.000 | 3 | 2015 | 2016 | |||||||||
|
0.882 | 0.120 | 1 | 11117039 | missense variant | C/T | snv |
|
0.800 | 1.000 | 3 | 2015 | 2016 | |||||||||
|
0.925 | 0.080 | 1 | 11195977 | 3 prime UTR variant | T/C | snv | 9.0E-02 |
|
0.020 | 1.000 | 2 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 1 | 11195977 | 3 prime UTR variant | T/C | snv | 9.0E-02 |
|
0.020 | 1.000 | 2 | 2013 | 2017 | ||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2014 | 2016 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2016 | 2019 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2012 | 2013 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2012 | 2013 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2016 | 2019 | |||||||||
|
0.827 | 0.240 | 1 | 11130747 | missense variant | C/T | snv |
|
0.020 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
0.827 | 0.240 | 1 | 11130747 | missense variant | C/T | snv |
|
0.020 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
0.827 | 0.240 | 1 | 11130747 | missense variant | C/T | snv |
|
0.020 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2013 | 2013 |