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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.080 | 7 | 44149977 | missense variant | G/A;T | snv | 8.0E-06 | 0.700 | 1.000 | 12 | 2000 | 2012 | ||||
|
29 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 0.700 | 1.000 | 12 | 1991 | 2013 | |||||
|
3 | 0.882 | 0.080 | 7 | 44153325 | missense variant | C/T | snv | 0.720 | 1.000 | 8 | 1998 | 2016 | |||||
|
93 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 0.070 | 1.000 | 7 | 2006 | 2020 | |||||
|
2 | 0.925 | 0.080 | 20 | 44424123 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 1.000 | 6 | 2000 | 2016 | ||||
|
6 | 0.807 | 0.200 | 12 | 120994265 | missense variant | G/A | snv | 0.700 | 1.000 | 6 | 1997 | 2009 | |||||
|
4 | 0.851 | 0.080 | 7 | 44153381 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 1.000 | 6 | 2002 | 2014 | ||||
|
2 | 0.925 | 0.080 | 7 | 44145173 | missense variant | G/A;T | snv | 4.2E-06 | 0.700 | 1.000 | 5 | 2003 | 2012 | ||||
|
2 | 0.925 | 0.080 | 11 | 2159907 | missense variant | T/C | snv | 0.700 | 1.000 | 5 | 2007 | 2015 | |||||
|
2 | 0.925 | 0.080 | 11 | 2159895 | missense variant | G/C | snv | 0.700 | 1.000 | 5 | 2007 | 2015 | |||||
|
6 | 0.807 | 0.280 | 1 | 156136009 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 5 | 1990 | 2013 | ||||
|
3 | 0.882 | 0.080 | 7 | 44147834 | splice acceptor variant | C/T | snv | 0.700 | 1.000 | 4 | 2003 | 2009 | |||||
|
2 | 0.925 | 0.080 | 20 | 44414663 | splice donor variant | G/A | snv | 0.700 | 1.000 | 4 | 1977 | 2013 | |||||
|
2 | 0.925 | 0.040 | 11 | 17387395 | missense variant | G/A | snv | 0.700 | 1.000 | 4 | 2011 | 2016 | |||||
|
2 | 0.925 | 0.080 | 20 | 44407421 | stop gained | C/T | snv | 0.700 | 1.000 | 4 | 2000 | 2013 | |||||
|
3 | 0.882 | 0.120 | 18 | 60371884 | stop gained | G/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 4 | 1999 | 2017 | ||||
|
3 | 0.882 | 0.080 | 7 | 44145495 | splice donor variant | A/T | snv | 0.700 | 1.000 | 3 | 2003 | 2009 | |||||
|
2 | 0.925 | 0.080 | 7 | 44146466 | missense variant | T/C | snv | 0.700 | 1.000 | 3 | 2006 | 2011 | |||||
|
3 | 0.882 | 0.080 | 7 | 44147765 | missense variant | G/A | snv | 0.700 | 1.000 | 3 | 2007 | 2009 | |||||
|
2 | 0.925 | 0.080 | 7 | 44153396 | missense variant | T/G | snv | 0.700 | 1.000 | 3 | 2000 | 2014 | |||||
|
2 | 0.925 | 0.080 | 12 | 120996261 | splice acceptor variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2009 | 2013 | |||||
|
4 | 0.882 | 0.080 | 7 | 44147726 | missense variant | A/G | snv | 7.0E-06 | 0.700 | 1.000 | 3 | 2002 | 2012 | ||||
|
2 | 0.925 | 0.080 | 7 | 44147795 | missense variant | T/C | snv | 0.700 | 1.000 | 2 | 2008 | 2015 | |||||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.020 | 1.000 | 2 | 2006 | 2011 | ||||
|
131 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.020 | 1.000 | 2 | 2006 | 2018 |