| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv |
|
0.900 | 0.952 | 21 | 2009 | 2020 | |||||||||
|
0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 |
|
0.900 | 0.889 | 18 | 2009 | 2020 | ||||||||
|
0.776 | 0.240 | 11 | 118606652 | 5 prime UTR variant | A/G;T | snv |
|
0.900 | 0.941 | 17 | 2009 | 2020 | |||||||||
|
0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 |
|
0.900 | 0.875 | 16 | 2009 | 2020 | ||||||||
|
0.763 | 0.200 | 8 | 129673211 | intron variant | T/G | snv | 0.17 |
|
0.900 | 1.000 | 12 | 2009 | 2020 | ||||||||
|
0.882 | 0.040 | 7 | 54911231 | intergenic variant | C/T | snv | 0.27 |
|
0.860 | 0.833 | 6 | 2011 | 2017 | ||||||||
|
0.882 | 0.040 | 7 | 55091656 | intron variant | A/G;T | snv | 0.20 |
|
0.850 | 1.000 | 6 | 2011 | 2018 | ||||||||
|
0.667 | 0.560 | 5 | 1288432 | intron variant | T/A;C | snv |
|
0.840 | 1.000 | 6 | 2009 | 2017 | |||||||||
|
0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 |
|
0.820 | 1.000 | 5 | 2009 | 2019 | ||||||||
|
0.763 | 0.080 | 20 | 63680946 | intron variant | T/C | snv | 0.81 |
|
0.820 | 1.000 | 5 | 2009 | 2018 | ||||||||
|
0.882 | 0.040 | 3 | 169862183 | intron variant | G/A | snv | 0.25 |
|
0.820 | 1.000 | 2 | 2014 | 2015 | ||||||||
|
0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 |
|
0.810 | 1.000 | 4 | 2009 | 2016 | ||||||||
|
0.851 | 0.120 | 8 | 129479506 | intron variant | T/G | snv | 0.17 |
|
0.810 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 49 | 2009 | 2019 | ||||||||
|
0.807 | 0.200 | 20 | 63686867 | non coding transcript exon variant | T/C | snv | 8.8E-02 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.732 | 0.080 | 8 | 129633446 | intron variant | A/G | snv | 3.9E-02 |
|
0.760 | 1.000 | 9 | 2013 | 2019 | ||||||||
|
0.882 | 0.040 | 8 | 129629675 | intron variant | A/G | snv | 0.18 |
|
0.720 | 1.000 | 4 | 2009 | 2019 | ||||||||
|
0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 |
|
0.720 | 1.000 | 4 | 2012 | 2018 | ||||||||
|
0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv |
|
0.720 | 1.000 | 2 | 2011 | 2012 | |||||||||
|
0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv |
|
0.710 | 1.000 | 3 | 2009 | 2018 | |||||||||
|
0.827 | 0.080 | 11 | 118657714 | 3 prime UTR variant | C/T | snv | 0.18 |
|
0.710 | 1.000 | 3 | 2009 | 2012 | ||||||||
|
0.851 | 0.080 | 9 | 22032153 | intron variant | T/G | snv | 0.28 |
|
0.710 | 1.000 | 3 | 2017 | 2019 | ||||||||
|
1.000 | 0.040 | 3 | 66452557 | intron variant | A/C;G | snv |
|
0.710 | 1.000 | 2 | 2017 | 2018 | |||||||||
|
0.882 | 0.040 | 15 | 76286421 | missense variant | G/A | snv | 7.4E-02 | 6.4E-02 |
|
0.710 | 1.000 | 2 | 2015 | 2017 | |||||||
|
0.701 | 0.360 | 9 | 22034720 | non coding transcript exon variant | G/A | snv | 0.46 |
|
0.710 | 1.000 | 2 | 2011 | 2019 |