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 | 1.000 | 0.120 | 14 | 64352051 | non coding transcript exon variant | G/A | snv | 0.45 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
4 | 1 | 22907986 | missense variant | G/T | snv | 4.0E-06 | 2.1E-05 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
2 | 1.000 | 0.040 | 19 | 45351661 | stop gained | T/A;G | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
10 | 0.851 | 0.080 | 2 | 29220747 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
3 | 1.000 | 0.080 | 8 | 143813896 | missense variant | T/C;G | snv | 6.1E-04 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 5 | 179705693 | missense variant | G/C | snv | 8.2E-06 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
4 | 0.882 | 0.080 | 11 | 102955629 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
4 | 0.882 | 0.080 | 1 | 39954534 | upstream gene variant | C/A | snv | 6.1E-02 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
101 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
12 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
63 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||||
|
4 | 0.882 | 0.080 | 16 | 55479556 | missense variant | A/G;T | snv | 4.1E-06 | 2.1E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
1 | 17 | 1456106 | missense variant | G/C | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||||
|
5 | 14 | 64236875 | intron variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
134 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
9 | 0.807 | 0.080 | 19 | 1206957 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
19 | 0.732 | 0.200 | 10 | 129467281 | synonymous variant | C/T | snv | 5.5E-02 | 5.1E-02 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||
|
72 | 0.557 | 0.640 | 19 | 45364001 | missense variant | C/A;T | snv | 7.1E-06; 0.29 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
4 | 0.925 | 0.120 | 4 | 88132618 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
11 | 0.807 | 0.120 | 15 | 78617197 | intron variant | G/T | snv | 0.61 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
23 | 0.677 | 0.280 | 17 | 7674217 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 1997 | 1997 | |||||
|
6 | 0.827 | 0.200 | 15 | 78573083 | intron variant | T/A;C | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
4 | 0.882 | 0.080 | 3 | 18430796 | intron variant | A/G | snv | 8.0E-02 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
29 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
2 | 1.000 | 0.040 | 1 | 22910452 | missense variant | T/A;G | snv | 2.8E-05; 4.0E-06 | 0.010 | 1.000 | 1 | 2015 | 2015 |