| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.742 | 0.200 | 9 | 97793827 | intron variant | A/G;T | snv |
|
0.860 | 1.000 | 5 | 2009 | 2016 | |||||||||
|
0.742 | 0.200 | 14 | 36180040 | upstream gene variant | C/T | snv | 0.45 |
|
0.850 | 1.000 | 1 | 2009 | 2015 | ||||||||
|
0.776 | 0.120 | 14 | 36269155 | regulatory region variant | C/T | snv | 2.3E-02 |
|
0.840 | 0.800 | 2 | 2012 | 2017 | ||||||||
|
0.776 | 0.200 | 8 | 32574851 | intron variant | G/C | snv | 0.54 |
|
0.830 | 1.000 | 1 | 2012 | 2015 | ||||||||
|
0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv |
|
0.820 | 1.000 | 1 | 2012 | 2013 | |||||||||
|
1.000 | 0.080 | 9 | 97775520 | intron variant | A/C | snv | 0.72 |
|
0.800 | 1.000 | 2 | 2010 | 2017 | ||||||||
|
0.882 | 0.080 | 9 | 97784318 | intron variant | C/T | snv | 0.71 |
|
0.800 | 1.000 | 2 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 217406996 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.776 | 0.160 | 9 | 97853632 | 5 prime UTR variant | A/G | snv | 0.63 |
|
0.750 | 1.000 | 1 | 2009 | 2015 | ||||||||
|
0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 |
|
0.720 | 1.000 | 1 | 2016 | 2019 | ||||||||
|
0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 |
|
0.710 | 1.000 | 3 | 2001 | 2018 | ||||||||
|
0.827 | 0.200 | 9 | 97786731 | intron variant | A/G | snv | 0.72 |
|
0.710 | 1.000 | 2 | 2010 | 2015 | ||||||||
|
0.851 | 0.080 | 9 | 97855197 | 3 prime UTR variant | G/T | snv | 0.63 |
|
0.710 | 1.000 | 1 | 2009 | 2015 | ||||||||
|
0.882 | 0.080 | 9 | 97896036 | regulatory region variant | A/G | snv | 0.71 |
|
0.710 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.080 | 9 | 97860315 | downstream gene variant | T/A;C;G | snv |
|
0.710 | 1.000 | 1 | 2009 | 2015 | |||||||||
|
0.925 | 0.080 | 9 | 97794690 | intron variant | A/G | snv | 0.72 |
|
0.700 | 1.000 | 3 | 2009 | 2013 | ||||||||
|
0.925 | 0.080 | 9 | 97874116 | regulatory region variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2009 | 2013 | |||||||||
|
1.000 | 0.080 | 9 | 97865986 | intergenic variant | G/A | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 9 | 97775173 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.925 | 0.080 | 9 | 97876993 | TF binding site variant | A/C | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 2 | 217427435 | non coding transcript exon variant | C/A;G | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 1 | 233276815 | intron variant | A/G | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.925 | 0.120 | 9 | 97846400 | intron variant | G/A | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 9 | 97855301 | 3 prime UTR variant | T/C | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.080 | 9 | 97787746 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 |