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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.060 | 0.833 | 6 | 2006 | 2018 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.040 | 0.750 | 4 | 2006 | 2015 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.030 | 1.000 | 3 | 2003 | 2012 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.030 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.030 | 0.667 | 3 | 2003 | 2014 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.030 | 1.000 | 3 | 2005 | 2009 | ||||||||
|
0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv |
|
0.020 | 1.000 | 2 | 2014 | 2018 | |||||||||
|
0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv |
|
0.020 | 1.000 | 2 | 2014 | 2016 | |||||||||
|
0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv |
|
0.020 | 1.000 | 2 | 2006 | 2018 | |||||||||
|
0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv |
|
0.020 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
0.742 | 0.200 | 7 | 101126257 | upstream gene variant | A/G | snv | 0.54 |
|
0.020 | 1.000 | 2 | 2006 | 2018 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2005 | 2009 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 0.500 | 2 | 2013 | 2015 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 0.500 | 2 | 2007 | 2017 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2007 | 2019 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2005 | 2014 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | < 0.001 | 2 | 2011 | 2014 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 1997 | 2009 | ||||||||
|
0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 |
|
0.020 | 0.500 | 2 | 2014 | 2018 | ||||||||
|
1.000 | 0.080 | 7 | 101137084 | splice donor variant | G/- | delins | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.200 | 7 | 101131931 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2002 | 2002 | |||||||||
|
0.882 | 0.200 | 7 | 101131931 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2002 | 2002 | |||||||||
|
0.882 | 0.200 | 7 | 101131931 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2002 | 2002 | |||||||||
|
1.000 | 0.040 | 7 | 101133793 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2010 | 2010 |