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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.882 | 0.080 | 15 | 74723851 | intron variant | G/A;C;T | snv | 0.21 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.080 | 15 | 74723851 | intron variant | G/A;C;T | snv | 0.21 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.080 | 15 | 74723851 | intron variant | G/A;C;T | snv | 0.21 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.100 | 0.900 | 20 | 1998 | 2017 | |||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.100 | 0.900 | 20 | 1998 | 2017 | |||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.100 | 0.900 | 20 | 1998 | 2017 | |||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.090 | 1.000 | 9 | 2012 | 2018 | |||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.090 | 1.000 | 9 | 2012 | 2018 | |||||||
|
0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 |
|
0.090 | 1.000 | 9 | 2012 | 2018 |