Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.851 | 0.120 | 7 | 150952514 | missense variant | C/G;T | snv | 0.730 | 1.000 | 5 | 2001 | 2013 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951738 | missense variant | A/G | snv | 7.2E-05 | 5.6E-05 | 0.720 | 1.000 | 6 | 2000 | 2014 | |||
|
3 | 0.882 | 0.200 | 7 | 150951679 | missense variant | C/A;G;T | snv | 0.720 | 1.000 | 6 | 2000 | 2016 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951615 | missense variant | A/C;G;T | snv | 4.0E-06 | 0.720 | 1.000 | 2 | 1996 | 2005 | ||||
|
3 | 0.882 | 0.120 | 7 | 150951583 | missense variant | C/T | snv | 0.710 | 1.000 | 14 | 1999 | 2014 | |||||
|
2 | 0.925 | 0.120 | 7 | 150974851 | missense variant | C/A;T | snv | 0.710 | 1.000 | 10 | 1999 | 2015 | |||||
|
4 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 0.710 | 1.000 | 9 | 1995 | 2013 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951793 | missense variant | G/A;T | snv | 0.710 | 1.000 | 9 | 1998 | 2019 | |||||
|
3 | 0.925 | 0.120 | 7 | 150951484 | missense variant | C/T | snv | 0.710 | 1.000 | 6 | 2002 | 2014 | |||||
|
4 | 0.925 | 0.160 | 7 | 150948861 | stop gained | G/A | snv | 4.0E-06 | 0.710 | 0.800 | 5 | 2003 | 2012 | ||||
|
4 | 0.851 | 0.120 | 7 | 150951643 | missense variant | C/A;G;T | snv | 8.0E-06 | 0.710 | 1.000 | 4 | 2000 | 2019 | ||||
|
6 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 0.710 | 1.000 | 1 | 2018 | 2018 | |||||
|
3 | 0.882 | 0.120 | 7 | 150950311 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.710 | 1.000 | 1 | 2003 | 2003 | |||
|
3 | 0.882 | 0.120 | 7 | 150950336 | stop gained | G/A;C;T | snv | 1.6E-05; 4.0E-06 | 0.710 | 1.000 | 1 | 2012 | 2012 | ||||
|
2 | 0.925 | 0.120 | 7 | 150951702 | missense variant | A/G;T | snv | 0.710 | 1.000 | 1 | 2000 | 2000 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951562 | missense variant | A/C;G | snv | 0.710 | 1.000 | 1 | 2005 | 2005 | |||||
|
3 | 0.882 | 0.120 | 7 | 150958449 | missense variant | G/A;C | snv | 3.2E-04 | 0.710 | 1.000 | 1 | 2006 | 2006 | ||||
|
2 | 0.925 | 0.120 | 7 | 150950167 | splice donor variant | C/A;G | snv | 0.710 | 1.000 | 1 | 2008 | 2008 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951552 | missense variant | G/A | snv | 0.700 | 1.000 | 30 | 1997 | 2015 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951507 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 14 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.120 | 7 | 150974920 | missense variant | T/G | snv | 0.700 | 1.000 | 13 | 1999 | 2017 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951555 | missense variant | G/A | snv | 0.700 | 1.000 | 13 | 1999 | 2015 | |||||
|
5 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 0.700 | 1.000 | 9 | 1998 | 2015 | |||||
|
2 | 0.925 | 0.120 | 7 | 150974809 | missense variant | T/C | snv | 0.700 | 1.000 | 9 | 1999 | 2014 | |||||
|
3 | 0.882 | 0.120 | 7 | 150950312 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 1.000 | 8 | 2000 | 2018 |