| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.080 | 12 | 6276561 | intergenic variant | C/T | snv | 0.84 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.790 | 0.080 | 1 | 183112059 | intron variant | A/C | snv | 0.37 |
|
0.800 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.790 | 0.080 | 10 | 99529178 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 2 | 2014 | 2016 | |||||||||
|
0.790 | 0.080 | 17 | 897353 | intron variant | T/C | snv | 2.3E-02 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 |
|
0.800 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
1.000 | 0.080 | MT | 7275 | missense variant | T/C | snv |
|
0.800 | 1.000 | 2 | 2006 | 2009 | |||||||||
|
1.000 | 0.080 | MT | 6277 | missense variant | G/A | snv |
|
0.800 | 1.000 | 2 | 2006 | 2009 | |||||||||
|
0.677 | 0.320 | 11 | 61796827 | 3 prime UTR variant | G/C;T | snv |
|
0.800 | 1.000 | 2 | 2014 | 2019 | |||||||||
|
0.790 | 0.080 | 10 | 58811675 | intron variant | C/T | snv | 0.53 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.763 | 0.160 | 2 | 191722478 | intron variant | T/C | snv | 0.16 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.080 | 4 | 93965880 | intergenic variant | T/C | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.080 | 19 | 33036982 | intron variant | T/C | snv | 0.18 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 8 | 116562277 | intergenic variant | C/G | snv | 9.8E-03 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.752 | 0.160 | 10 | 116727589 | intron variant | T/C | snv | 0.69 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.080 | 12 | 4296223 | intron variant | A/G | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.080 | 12 | 50179650 | intron variant | G/C | snv | 0.37 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.708 | 0.320 | 1 | 114716124 | missense variant | C/A;G;T | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | 4 | 1803725 | missense variant | G/A | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | 5 | 113043623 | missense variant | G/A | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | 5 | 113064110 | missense variant | C/T | snv | 1.2E-05 |
|
0.800 | 0 | |||||||||||
|
1.000 | 0.080 | MT | 8009 | missense variant | G/A | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | MT | 15572 | missense variant | T/C | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | MT | 10563 | missense variant | T/C | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | 22 | 41178373 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.800 | 0 | |||||||||||
|
1.000 | 0.080 | 18 | 53526629 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 |
|
0.800 | 0 |