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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.240 | 6 | 28808340 | intergenic variant | G/A | snv | 7.2E-02 |
|
0.040 | 1.000 | 4 | 2010 | 2017 | ||||||||
|
0.630 | 0.640 | 15 | 74719300 | downstream gene variant | A/G;T | snv | 0.18 |
|
0.040 | 0.750 | 4 | 2010 | 2016 | ||||||||
|
0.742 | 0.240 | 15 | 78596058 | 3 prime UTR variant | G/A | snv | 0.39 |
|
0.040 | 1.000 | 4 | 2010 | 2020 | ||||||||
|
0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv |
|
0.040 | 1.000 | 4 | 2009 | 2014 | |||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.040 | 1.000 | 4 | 2008 | 2017 | ||||||||
|
0.701 | 0.400 | 15 | 74749576 | intron variant | C/A | snv | 0.67 |
|
0.040 | 1.000 | 4 | 2012 | 2014 | ||||||||
|
0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv |
|
0.030 | 1.000 | 3 | 2010 | 2012 | |||||||||
|
0.672 | 0.480 | 14 | 20454990 | non coding transcript exon variant | T/C;G | snv |
|
0.030 | 1.000 | 3 | 2009 | 2014 | |||||||||
|
0.658 | 0.480 | 6 | 32184610 | upstream gene variant | A/G;T | snv |
|
0.030 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 |
|
0.030 | 0.667 | 3 | 2014 | 2018 | ||||||||
|
0.695 | 0.240 | 10 | 133526341 | non coding transcript exon variant | C/T | snv | 3.1E-02 |
|
0.030 | 1.000 | 3 | 2012 | 2016 | ||||||||
|
0.653 | 0.400 | 19 | 45423658 | intron variant | C/A;T | snv |
|
0.030 | 1.000 | 3 | 2011 | 2014 | |||||||||
|
0.851 | 0.080 | 13 | 91792975 | intron variant | C/G;T | snv |
|
0.030 | 1.000 | 3 | 2010 | 2015 | |||||||||
|
0.649 | 0.320 | 5 | 1295234 | upstream gene variant | A/G | snv | 0.25 |
|
0.030 | 1.000 | 3 | 2013 | 2018 | ||||||||
|
0.827 | 0.120 | 7 | 76301442 | upstream gene variant | C/G | snv | 0.22 |
|
0.030 | 0.667 | 3 | 2015 | 2019 | ||||||||
|
0.807 | 0.120 | 15 | 78617197 | intron variant | G/T | snv | 0.61 |
|
0.030 | 0.667 | 3 | 2010 | 2013 | ||||||||
|
0.776 | 0.200 | 5 | 1320132 | intron variant | G/A | snv | 0.47 |
|
0.710 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.160 | 1 | 15524988 | intron variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2010 | 2013 | |||||||||
|
0.807 | 0.160 | 11 | 108354934 | 3 prime UTR variant | A/G;T | snv |
|
0.030 | 1.000 | 3 | 2012 | 2017 | |||||||||
|
0.807 | 0.160 | 11 | 108272455 | intron variant | C/A;T | snv | 0.65 |
|
0.030 | 1.000 | 3 | 2012 | 2017 | ||||||||
|
0.763 | 0.160 | 10 | 112738717 | intron variant | G/A | snv | 0.20 |
|
0.720 | 1.000 | 3 | 2012 | 2018 | ||||||||
|
0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv |
|
0.030 | 1.000 | 3 | 2014 | 2017 | |||||||||
|
0.851 | 0.080 | 15 | 78533838 | 3 prime UTR variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2009 | 2015 | |||||||||
|
0.701 | 0.320 | 6 | 30374976 | intergenic variant | G/A | snv |
|
0.700 | 1.000 | 2 | 2016 | 2017 | |||||||||
|
0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv |
|
0.020 | 1.000 | 2 | 2016 | 2019 |