| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 |
|
0.900 | 1.000 | 20 | 2011 | 2019 | ||||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
0.900 | 0.833 | 12 | 2010 | 2019 | ||||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
0.900 | 0.909 | 11 | 2013 | 2019 | ||||||||
|
0.807 | 0.200 | 6 | 32698518 | intergenic variant | A/G | snv | 0.15 |
|
0.850 | 0.800 | 5 | 2013 | 2018 | ||||||||
|
0.724 | 0.360 | 6 | 32711222 | upstream gene variant | A/G;T | snv |
|
0.840 | 1.000 | 6 | 2011 | 2017 | |||||||||
|
0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv |
|
0.820 | 1.000 | 3 | 2016 | 2018 | |||||||||
|
1.000 | 0.080 | 3 | 32978543 | intergenic variant | G/T | snv | 0.73 |
|
0.810 | 1.000 | 3 | 2010 | 2016 | ||||||||
|
0.763 | 0.240 | 3 | 41224645 | missense variant | T/C;G | snv |
|
0.810 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
0.763 | 0.240 | 3 | 41224634 | missense variant | C/A;T | snv |
|
0.810 | 1.000 | 2 | 2015 | 2016 | |||||||||
|
0.925 | 0.120 | 6 | 32632222 | intron variant | G/A | snv | 0.55 |
|
0.810 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
1.000 | 0.080 | 21 | 29773850 | intron variant | A/C;G | snv |
|
0.810 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.645 | 0.360 | 17 | 7674216 | missense variant | C/A;G | snv |
|
0.800 | 1.000 | 22 | 1994 | 2020 | |||||||||
|
0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv |
|
0.800 | 1.000 | 2 | 2005 | 2016 | |||||||||
|
0.742 | 0.200 | 3 | 41224621 | missense variant | T/C;G | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.732 | 0.200 | 3 | 41224607 | missense variant | A/C;G;T | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.724 | 0.200 | 3 | 41224612 | missense variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.683 | 0.360 | 3 | 41224610 | missense variant | C/A;G;T | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.683 | 0.240 | 3 | 41224622 | missense variant | C/A;G;T | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.200 | 3 | 41224606 | missense variant | G/A;C;T | snv |
|
0.800 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.827 | 0.160 | 22 | 31869917 | intron variant | T/G | snv | 0.37 |
|
0.760 | 1.000 | 7 | 2013 | 2019 | ||||||||
|
0.790 | 0.360 | 6 | 32702478 | downstream gene variant | C/T | snv | 0.34 |
|
0.750 | 1.000 | 6 | 2012 | 2017 | ||||||||
|
0.701 | 0.440 | 6 | 33065245 | 3 prime UTR variant | A/G | snv | 0.29 |
|
0.740 | 0.600 | 5 | 2011 | 2015 | ||||||||
|
0.752 | 0.440 | 6 | 32762235 | intron variant | A/G;T | snv |
|
0.740 | 0.800 | 5 | 2012 | 2018 | |||||||||
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
0.740 | 0.800 | 5 | 2012 | 2015 |