| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.732 | 0.520 | 16 | 31265490 | missense variant | G/A | snv | 9.7E-02 | 0.11 |
|
0.900 | 1.000 | 1 | 2009 | 2019 | |||||||
|
0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 |
|
0.880 | 1.000 | 1 | 2008 | 2019 | ||||||||
|
0.807 | 0.280 | 4 | 101829765 | intron variant | T/C | snv | 0.25 | 0.27 |
|
0.850 | 1.000 | 1 | 2008 | 2017 | |||||||
|
0.701 | 0.440 | 6 | 137874586 | intron variant | C/G | snv | 0.13 |
|
0.850 | 1.000 | 1 | 2008 | 2017 | ||||||||
|
0.776 | 0.240 | 5 | 160452971 | intron variant | T/C | snv | 0.44 |
|
0.840 | 1.000 | 1 | 2008 | 2017 | ||||||||
|
0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 |
|
0.840 | 1.000 | 1 | 2009 | 2019 | ||||||||
|
0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv |
|
0.830 | 1.000 | 1 | 2009 | 2017 | |||||||||
|
0.807 | 0.360 | 7 | 50266267 | upstream gene variant | T/G | snv | 0.26 |
|
0.830 | 1.000 | 1 | 2009 | 2017 | ||||||||
|
0.882 | 0.120 | 11 | 589564 | intron variant | T/C | snv | 0.64 |
|
0.830 | 1.000 | 1 | 2008 | 2012 | ||||||||
|
0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 |
|
0.830 | 1.000 | 1 | 2009 | 2017 | ||||||||
|
0.851 | 0.160 | 3 | 58384450 | intron variant | G/T | snv | 0.63 |
|
0.830 | 1.000 | 1 | 2008 | 2012 | ||||||||
|
0.882 | 0.200 | 16 | 31357553 | missense variant | T/C | snv | 0.21 |
|
0.820 | 1.000 | 1 | 2008 | 2011 | ||||||||
|
0.925 | 0.120 | 4 | 87037243 | intron variant | G/A | snv | 0.42 |
|
0.820 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 1 | 173340574 | intergenic variant | A/G;T | snv |
|
0.810 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.851 | 0.160 | 11 | 128459064 | 3 prime UTR variant | C/T | snv | 0.11 |
|
0.810 | 1.000 | 1 | 2010 | 2016 | ||||||||
|
0.851 | 0.200 | 6 | 32082981 | intron variant | C/A;T | snv |
|
0.810 | 1.000 | 1 | 2011 | 2017 | |||||||||
|
0.925 | 0.160 | 16 | 11096031 | intron variant | T/C | snv | 0.51 |
|
0.810 | 1.000 | 1 | 2011 | 2013 | ||||||||
|
0.882 | 0.200 | 2 | 33476823 | intron variant | T/C | snv | 6.3E-02 |
|
0.810 | 1.000 | 1 | 2009 | 2017 | ||||||||
|
0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 |
|
0.810 | 1.000 | 1 | 2008 | 2017 | ||||||||
|
0.925 | 0.120 | 11 | 118702810 | intron variant | T/C | snv | 0.23 |
|
0.810 | 1.000 | 1 | 2009 | 2012 | ||||||||
|
0.925 | 0.120 | 10 | 62045858 | intron variant | T/C | snv | 0.55 |
|
0.810 | 1.000 | 1 | 2013 | 2016 | ||||||||
|
1.000 | 0.080 | 3 | 119542097 | intron variant | A/G | snv | 0.17 |
|
0.810 | 1.000 | 1 | 2013 | 2016 | ||||||||
|
0.851 | 0.240 | 1 | 173257056 | intergenic variant | T/G | snv | 0.29 |
|
0.810 | 1.000 | 1 | 2013 | 2016 | ||||||||
|
0.882 | 0.120 | 13 | 40983974 | intron variant | A/G | snv | 4.5E-02 |
|
0.810 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.160 | 2 | 191075725 | intron variant | G/A;T | snv |
|
0.810 | 1.000 | 1 | 2010 | 2013 |