| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv |
|
0.720 | 1.000 | 5 | 2013 | 2017 | |||||||||
|
0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv |
|
0.770 | 0.818 | 4 | 2009 | 2017 | |||||||||
|
0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 4 | 2007 | 2018 | |||||||||
|
0.925 | 0.080 | 5 | 58888234 | regulatory region variant | T/A;C | snv |
|
0.700 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.925 | 0.080 | 9 | 107543834 | upstream gene variant | C/A;T | snv |
|
0.710 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.925 | 0.080 | 11 | 129591276 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.882 | 0.080 | 3 | 30641447 | intron variant | G/C;T | snv |
|
0.710 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.925 | 0.080 | 2 | 19121042 | intron variant | T/A;C | snv |
|
0.710 | 1.000 | 3 | 2013 | 2017 | |||||||||
|
0.925 | 0.080 | 14 | 36663564 | intron variant | G/A;C | snv | 0.18; 8.6E-06 |
|
0.700 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.807 | 0.080 | 2 | 120487546 | intergenic variant | T/A;C | snv |
|
0.710 | 1.000 | 3 | 2013 | 2019 | |||||||||
|
0.851 | 0.080 | 9 | 108126198 | regulatory region variant | G/A;T | snv |
|
0.740 | 1.000 | 3 | 2011 | 2016 | |||||||||
|
0.851 | 0.080 | 6 | 151597721 | intron variant | T/C;G | snv |
|
0.710 | 1.000 | 2 | 2012 | 2016 | |||||||||
|
1.000 | 0.080 | 5 | 16187419 | downstream gene variant | G/A;C;T | snv |
|
0.700 | 1.000 | 2 | 2015 | 2017 | |||||||||
|
0.597 | 0.480 | 22 | 28725099 | missense variant | A/C;G | snv | 4.1E-03 |
|
0.900 | 0.895 | 2 | 2003 | 2017 | ||||||||
|
0.925 | 0.080 | 10 | 121580797 | intron variant | C/A;T | snv |
|
0.790 | 0.909 | 2 | 2009 | 2018 | |||||||||
|
0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 |
|
0.730 | 0.800 | 2 | 2013 | 2018 | ||||||||
|
0.925 | 0.080 | 11 | 69516874 | regulatory region variant | C/A;G;T | snv |
|
0.710 | 1.000 | 2 | 2013 | 2017 | |||||||||
|
1.000 | 0.080 | 8 | 220692 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 2 | 2017 | 2017 | |||||||||
|
0.882 | 0.080 | 3 | 46825376 | downstream gene variant | G/A;T | snv |
|
0.700 | 1.000 | 2 | 2015 | 2017 | |||||||||
|
1.000 | 0.080 | 6 | 28958443 | TF binding site variant | G/A;C;T | snv |
|
0.700 | 1.000 | 2 | 2015 | 2017 | |||||||||
|
0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 1 | 155446537 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 1 | 10503552 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1.000 | 0.080 | 10 | 13865236 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 1 | 118488075 | regulatory region variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 |