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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.160 | 11 | 41893816 | intergenic variant | C/A | snv | 9.8E-02 |
|
0.840 | 1.000 | 1 | 2007 | 2011 | ||||||||
|
1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 |
|
0.820 | 1.000 | 8 | 2008 | 2019 | ||||||||
|
0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 |
|
0.900 | 1.000 | 6 | 2008 | 2019 | ||||||||
|
0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 |
|
0.880 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.882 | 0.120 | 3 | 64726228 | intron variant | C/T | snv | 0.28 |
|
0.840 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.770 | 1.000 | 2 | 2008 | 2019 | |||||||
|
0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv |
|
0.900 | 0.889 | 2 | 2008 | 2019 | |||||||||
|
0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 |
|
0.840 | 1.000 | 2 | 2008 | 2017 | |||||||
|
0.763 | 0.320 | 7 | 28140937 | intron variant | T/C | snv | 0.41 |
|
0.890 | 0.929 | 2 | 2008 | 2017 | ||||||||
|
0.925 | 0.120 | 12 | 54705212 | intergenic variant | T/A | snv | 0.76 |
|
0.810 | 1.000 | 1 | 2008 | 2012 | ||||||||
|
0.882 | 0.120 | 10 | 12286011 | intergenic variant | A/G | snv | 0.17 |
|
0.850 | 1.000 | 1 | 2008 | 2015 | ||||||||
|
0.925 | 0.120 | 3 | 12236345 | regulatory region variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2008 | 2011 | |||||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
0.830 | 0.750 | 1 | 2008 | 2013 | ||||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
0.730 | 1.000 | 1 | 2008 | 2018 | |||||||
|
0.925 | 0.120 | 6 | 20657634 | intron variant | A/G | snv | 0.40 |
|
0.820 | 1.000 | 1 | 2008 | 2019 | ||||||||
|
0.925 | 0.120 | 3 | 185812502 | intron variant | T/C | snv | 0.46 |
|
0.810 | 1.000 | 1 | 2008 | 2012 | ||||||||
|
0.925 | 0.120 | 9 | 22129580 | downstream gene variant | C/A;T | snv |
|
0.810 | 1.000 | 1 | 2008 | 2011 | |||||||||
|
0.827 | 0.200 | 12 | 71269322 | intron variant | C/T | snv | 0.75 |
|
0.840 | 1.000 | 1 | 2008 | 2017 | ||||||||
|
0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 |
|
0.900 | 0.939 | 6 | 2009 | 2020 | ||||||||
|
0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 |
|
0.840 | 1.000 | 4 | 2009 | 2018 | ||||||||
|
0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 |
|
0.730 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
0.882 | 0.120 | 9 | 22132077 | downstream gene variant | A/G;T | snv | 0.18 |
|
0.810 | 1.000 | 3 | 2009 | 2016 | ||||||||
|
0.790 | 0.280 | 17 | 37738049 | intron variant | A/G | snv | 0.52 |
|
0.870 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 |
|
0.760 | 1.000 | 2 | 2009 | 2017 | ||||||||
|
0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 |
|
0.820 | 1.000 | 2 | 2009 | 2017 |