| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.882 | 0.160 | 12 | 10159690 | 3 prime UTR variant | G/A | snv | 0.40 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 9 | 101884874 | intergenic variant | A/G | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 4 | 102133052 | intergenic variant | C/T | snv | 6.2E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 |
|
0.020 | 1.000 | 2 | 2010 | 2010 | |||||||
|
1.000 | 0.080 | 11 | 102284743 | intergenic variant | A/G | snv | 0.93 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.160 | 8 | 102296172 | intron variant | A/C | snv | 0.21 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.080 | 20 | 10245498 | intron variant | C/T | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 12 | 102475727 | missense variant | C/T | snv | 8.0E-06 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.790 | 0.240 | 20 | 10253609 | intron variant | G/A | snv | 0.57 |
|
0.020 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
1.000 | 0.080 | 4 | 102747187 | intron variant | T/G | snv | 0.29 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 11 | 102835973 | 3 prime UTR variant | C/T | snv | 2.0E-02 |
|
0.010 | 1.000 | 1 | 2005 | 2005 | ||||||||
|
0.925 | 0.120 | 10 | 102836092 | intron variant | G/A;C;T | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.672 | 0.360 | 10 | 102837395 | 5 prime UTR variant | A/G;T | snv | 0.40; 8.1E-06 |
|
0.020 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 |
|
0.010 | 1.000 | 1 | 2005 | 2005 | |||||||
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
0.010 | 1.000 | 1 | 2005 | 2005 | |||||||
|
1.000 | 0.080 | 11 | 102846249 | upstream gene variant | A/G | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
0.020 | 0.500 | 2 | 2003 | 2003 | |||||||
|
1.000 | 0.080 | 11 | 102862432 | downstream gene variant | T/C | snv | 0.12 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.851 | 0.160 | 4 | 102872408 | intron variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.851 | 0.160 | 4 | 102872502 | intron variant | T/A;C | snv |
|
0.010 | < 0.001 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.080 | 8 | 102963761 | intron variant | A/G | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 8 | 103359219 | intergenic variant | T/C | snv | 3.6E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |