| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 |
|
0.800 | 1.000 | 4 | 2008 | 2019 | ||||||||
|
1 | 62465961 | intron variant | C/A | snv | 0.57 |
|
0.800 | 1.000 | 2 | 2009 | 2019 | ||||||||||
|
1.000 | 0.080 | 1 | 62726106 | regulatory region variant | C/T | snv | 0.16 |
|
0.800 | 1.000 | 2 | 2008 | 2019 | ||||||||
|
0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2008 | 2019 | |||||||||
|
1 | 62590441 | intron variant | G/A | snv | 0.42 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
1 | 62560271 | intron variant | G/T | snv | 0.57 |
|
0.800 | 1.000 | 2 | 2010 | 2019 | ||||||||||
|
0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 |
|
0.800 | 1.000 | 2 | 2008 | 2018 | ||||||||
|
1 | 62606594 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1 | 62652525 | intron variant | A/C;T | snv |
|
0.800 | 1.000 | 1 | 2009 | 2019 | |||||||||||
|
1 | 162265600 | intron variant | C/T | snv | 0.97 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 62596235 | intron variant | C/T | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 67166721 | intron variant | T/G | snv | 2.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 204161105 | intron variant | C/A | snv | 5.0E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.120 | 1 | 62531167 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 1 | 2010 | 2019 | |||||||||
|
1 | 27121557 | intron variant | G/A | snv | 6.0E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 27138426 | intron variant | A/G | snv | 1.9E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 54558033 | intron variant | A/G | snv | 6.0E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 62589609 | intron variant | G/A | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 156586027 | missense variant | A/G | snv | 1.1E-02 | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 78532228 | missense variant | C/A;T | snv | 3.5E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
1 | 162163356 | intron variant | G/A | snv | 0.96 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 240288305 | intron variant | G/C | snv | 3.0E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 103097312 | intron variant | T/G | snv | 0.96 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 46817672 | intron variant | G/T | snv | 1.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |