| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.120 | 5 | 10689450 | intron variant | T/G | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 19 | 10706980 | intron variant | T/C | snv | 0.73 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.925 | 0.040 | 19 | 10707416 | intron variant | G/A | snv | 0.57 | 0.59 |
|
0.800 | 1.000 | 2 | 2012 | 2015 | |||||||
|
0.827 | 0.120 | 7 | 107809588 | downstream gene variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.827 | 0.120 | 7 | 107839681 | regulatory region variant | A/T | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 9 | 108054739 | regulatory region variant | A/G | snv | 0.44 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.120 | 11 | 110085620 | intron variant | C/T | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.807 | 0.120 | 11 | 110091706 | intron variant | A/G | snv | 0.36 |
|
0.800 | 1.000 | 2 | 2012 | 2016 | ||||||||
|
0.827 | 0.120 | 16 | 11067551 | intron variant | G/C | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 6 | 111261682 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.040 | 6 | 111334327 | intron variant | G/A | snv | 8.7E-02 |
|
0.800 | 1.000 | 1 | 2010 | 2015 | ||||||||
|
1.000 | 0.040 | 6 | 111352511 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 3 | 2010 | 2015 | |||||||||
|
0.925 | 0.080 | 6 | 111374888 | missense variant | T/C | snv | 5.9E-02 | 5.6E-02 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 |
|
0.850 | 1.000 | 2 | 2010 | 2019 | |||||||
|
1.000 | 0.040 | 6 | 111605706 | intron variant | A/G | snv | 7.2E-02 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 6 | 111608659 | upstream gene variant | G/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.120 | 16 | 11225500 | downstream gene variant | C/T | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 19 | 1124032 | intron variant | G/A | snv | 0.24 | 0.26 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.882 | 0.120 | 16 | 11254001 | intron variant | T/C;G | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.807 | 0.120 | 16 | 11271643 | intron variant | C/T | snv | 0.32 |
|
0.800 | 1.000 | 2 | 2012 | 2016 | ||||||||
|
0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 |
|
0.710 | 1.000 | 1 | 2015 | 2017 | ||||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
0.740 | 0.800 | 1 | 2008 | 2016 |