| 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 | 0.080 | 10 | 62492218 | intron variant | C/T | snv | 0.42 |
|
0.720 | 1.000 | 1 | 2011 | 2016 | ||||||||
|
0.695 | 0.280 | 10 | 121575416 | intron variant | G/A;T | snv | 0.34 |
|
0.720 | 1.000 | 1 | 2012 | 2016 | ||||||||
|
0.925 | 0.080 | 16 | 52601088 | intron variant | C/T | snv | 0.19 |
|
0.720 | 1.000 | 1 | 2013 | 2019 | ||||||||
|
0.882 | 0.080 | 10 | 5844771 | upstream gene variant | C/T | snv | 0.47 |
|
0.720 | 1.000 | 1 | 2010 | 2012 | ||||||||
|
0.851 | 0.080 | 10 | 121573063 | intron variant | C/G;T | snv |
|
0.720 | 1.000 | 1 | 2009 | 2012 | |||||||||
|
0.827 | 0.160 | 6 | 151666222 | intron variant | G/T | snv | 0.11 |
|
0.720 | 1.000 | 1 | 2011 | 2014 | ||||||||
|
0.807 | 0.120 | 6 | 149287738 | intron variant | G/A | snv | 0.20 |
|
0.720 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.925 | 0.080 | 1 | 10506158 | intron variant | A/G | snv | 0.27 |
|
0.710 | 1.000 | 4 | 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 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 |
|
0.710 | 1.000 | 3 | 2013 | 2018 | |||||||
|
0.925 | 0.080 | 8 | 128182395 | intron variant | C/T | snv | 0.13 |
|
0.710 | 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 | 16 | 80616908 | intron variant | A/G | snv | 0.35 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 19 | 18460331 | intron variant | A/G | snv | 0.45 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.807 | 0.080 | 2 | 120487546 | intergenic variant | T/A;C | snv |
|
0.710 | 1.000 | 3 | 2013 | 2019 | |||||||||
|
0.925 | 0.080 | 22 | 40480230 | intron variant | T/C | snv | 0.12 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.882 | 0.080 | 11 | 69513996 | intergenic variant | C/T | snv | 0.14 |
|
0.710 | 1.000 | 3 | 2010 | 2014 | ||||||||
|
0.851 | 0.080 | 4 | 174925275 | intron variant | C/A | snv | 0.20 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 12 | 28021884 | TF binding site variant | C/T | snv | 0.22 |
|
0.710 | 1.000 | 3 | 2016 | 2017 | ||||||||
|
0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 |
|
0.710 | 1.000 | 3 | 2013 | 2018 | ||||||||
|
0.925 | 0.080 | 14 | 91374725 | intron variant | A/G | snv | 0.46 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 8 | 29652100 | intergenic variant | A/C | snv | 0.66 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 4 | 105163621 | intron variant | C/T | snv | 0.20 |
|
0.710 | 1.000 | 3 | 2013 | 2017 | ||||||||
|
0.925 | 0.080 | 5 | 91436408 | intron variant | C/T | snv | 0.23 |
|
0.710 | 1.000 | 2 | 2014 | 2017 |