| 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 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2014 | 2018 | ||||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
0.710 | 1.000 | 1 | 2013 | 2015 | ||||||||
|
0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.160 | 9 | 22024352 | intron variant | C/T | snv | 0.40 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.827 | 0.160 | 9 | 22019674 | intron variant | G/C | snv | 0.30 |
|
0.710 | 1.000 | 1 | 2007 | 2019 | ||||||||
|
0.827 | 0.080 | 9 | 22019130 | intron variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.851 | 0.120 | 6 | 160442500 | intron variant | T/C | snv | 0.28 |
|
0.700 | 1.000 | 3 | 2009 | 2014 | ||||||||
|
0.851 | 0.120 | 1 | 56497149 | intron variant | A/G | snv | 0.11 |
|
0.710 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.851 | 0.120 | 15 | 78849442 | intron variant | T/C | snv | 0.45 |
|
0.800 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.851 | 0.080 | 21 | 34226827 | intron variant | C/T | snv | 0.15 |
|
0.700 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
0.851 | 0.160 | 9 | 22098620 | intron variant | A/G | snv | 0.40 |
|
0.820 | 1.000 | 1 | 2007 | 2018 | ||||||||
|
0.851 | 0.080 | 14 | 99667605 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2013 | 2018 | |||||||||
|
0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 |
|
0.800 | 1.000 | 1 | 2014 | 2018 | ||||||||
|
0.851 | 0.080 | 2 | 202881162 | intron variant | T/C | snv | 8.9E-02 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 6 | 12901209 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv |
|
0.710 | 1.000 | 1 | 2007 | 2015 | |||||||||
|
0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 |
|
0.800 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 |
|
0.800 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.882 | 0.120 | 9 | 22029446 | missense variant | G/A | snv | 0.55 | 0.46 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.882 | 0.120 | 2 | 85582866 | upstream gene variant | C/T | snv | 0.52 |
|
0.810 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.882 | 0.120 | 15 | 90873320 | intron variant | C/A;G | snv |
|
0.810 | 1.000 | 1 | 2013 | 2018 | |||||||||
|
0.882 | 0.080 | 17 | 2214651 | intron variant | A/G | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.080 | 10 | 30046193 | intron variant | T/C | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2013 | 2013 |