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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.010 | < 0.001 | 1 | 2016 | 2016 | ||||||||
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.010 | < 0.001 | 1 | 2001 | 2001 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.010 | < 0.001 | 1 | 1999 | 1999 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.010 | < 0.001 | 1 | 2018 | 2018 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.807 | 0.160 | 13 | 46835532 | missense variant | C/A;T | snv | 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2012 | 2012 | ||||||||
|
13 | 46835363 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 |
|
0.010 | < 0.001 | 1 | 2013 | 2013 | |||||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.040 | 0.500 | 4 | 2001 | 2013 | |||||||
|
0.882 | 0.040 | 13 | 46892487 | synonymous variant | G/A | snv | 1.8E-02 | 1.7E-02 |
|
0.020 | 0.500 | 2 | 2007 | 2019 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.020 | 0.500 | 2 | 2010 | 2016 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.020 | 0.500 | 2 | 2001 | 2004 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.020 | 0.500 | 2 | 2001 | 2005 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.020 | 0.500 | 2 | 2001 | 2005 | |||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.050 | 0.600 | 5 | 1999 | 2012 | |||||||
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.030 | 0.667 | 3 | 2014 | 2019 | ||||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.030 | 0.667 | 3 | 2001 | 2006 | |||||||
|
0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 |
|
0.030 | 0.667 | 3 | 2000 | 2007 | |||||||
|
0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 |
|
0.100 | 0.800 | 10 | 2010 | 2019 | ||||||||
|
0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 |
|
0.050 | 0.800 | 5 | 2011 | 2015 |