| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.400 | 7 | 5978664 | missense variant | T/A;G | snv |
|
0.100 | 0.900 | 10 | 2008 | 2019 | |||||||||
|
0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv |
|
0.100 | 1.000 | 10 | 2004 | 2019 | |||||||||
|
0.683 | 0.360 | 3 | 41224610 | missense variant | C/A;G;T | snv |
|
0.800 | 1.000 | 10 | 2006 | 2015 | |||||||||
|
1.000 | 0.080 | 7 | 140781623 | missense variant | C/A | snv |
|
0.800 | 1.000 | 10 | 2006 | 2015 | |||||||||
|
1.000 | 0.080 | 7 | 140781620 | missense variant | A/C | snv |
|
0.800 | 1.000 | 10 | 2006 | 2015 | |||||||||
|
0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv |
|
0.100 | 0.800 | 10 | 2003 | 2010 | |||||||||
|
0.732 | 0.240 | 20 | 6423634 | intergenic variant | C/A | snv | 0.34 |
|
0.860 | 1.000 | 10 | 2008 | 2019 | ||||||||
|
0.653 | 0.400 | 3 | 36993455 | 5 prime UTR variant | G/A | snv | 0.22 |
|
0.090 | 0.778 | 9 | 2010 | 2019 | ||||||||
|
0.827 | 0.120 | 18 | 48932662 | intron variant | T/C | snv | 0.25 |
|
0.780 | 1.000 | 9 | 2007 | 2018 | ||||||||
|
0.732 | 0.240 | 8 | 127412547 | intron variant | A/G | snv | 0.63 |
|
0.830 | 0.889 | 9 | 2008 | 2019 | ||||||||
|
0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 |
|
0.840 | 1.000 | 8 | 2010 | 2019 | ||||||||
|
0.742 | 0.160 | 19 | 33041394 | intron variant | C/T | snv | 0.22 |
|
0.840 | 1.000 | 7 | 2008 | 2019 | ||||||||
|
0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 |
|
0.070 | 0.857 | 7 | 2013 | 2019 | ||||||||
|
0.776 | 0.080 | 10 | 79059375 | intron variant | A/G | snv | 0.55 |
|
0.810 | 1.000 | 7 | 2014 | 2019 | ||||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.820 | 0.833 | 6 | 2014 | 2019 | ||||||||
|
0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 |
|
0.810 | 1.000 | 6 | 2014 | 2019 | ||||||||
|
0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv |
|
0.060 | 0.833 | 6 | 2008 | 2017 | |||||||||
|
0.776 | 0.080 | 5 | 135163402 | intron variant | C/A | snv | 0.63 |
|
0.820 | 1.000 | 6 | 2013 | 2019 | ||||||||
|
0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 |
|
0.820 | 1.000 | 6 | 2014 | 2019 | ||||||||
|
0.732 | 0.160 | 16 | 68787043 | intron variant | G/A | snv | 0.28 |
|
0.850 | 1.000 | 6 | 2008 | 2016 | ||||||||
|
0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 |
|
0.050 | 1.000 | 5 | 2007 | 2018 | ||||||||
|
0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 |
|
0.810 | 1.000 | 5 | 2013 | 2019 | ||||||||
|
0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 |
|
0.730 | 1.000 | 5 | 2013 | 2019 | ||||||||
|
0.776 | 0.080 | 15 | 32700910 | downstream gene variant | C/T | snv | 0.11 |
|
0.720 | 1.000 | 5 | 2011 | 2019 | ||||||||
|
0.514 | 0.760 | 6 | 52186235 | upstream gene variant | G/A | snv | 0.28 |
|
0.050 | 1.000 | 5 | 2014 | 2019 |