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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.790 | 0.120 | 19 | 49154952 | missense variant | A/C | snv | 0.41 | 0.38 | 0.040 | 1.000 | 4 | 2011 | 2018 | |||
|
5 | 0.851 | 0.120 | 17 | 70175553 | missense variant | G/A | snv | 0.030 | 1.000 | 3 | 2005 | 2017 | |||||
|
10 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 0.030 | 1.000 | 3 | 2007 | 2014 | |||||
|
15 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2006 | 2017 | ||||
|
8 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 0.030 | 1.000 | 3 | 2009 | 2018 | |||||
|
4 | 0.925 | 0.120 | 11 | 2847899 | missense variant | G/A;T | snv | 6.2E-03 | 0.020 | 1.000 | 2 | 2014 | 2018 | ||||
|
18 | 0.724 | 0.280 | 7 | 150948446 | missense variant | T/A;C;G | snv | 1.3E-05; 0.18; 8.4E-06 | 0.020 | 1.000 | 2 | 2010 | 2017 | ||||
|
10 | 0.776 | 0.160 | 21 | 34449382 | missense variant | C/T | snv | 9.4E-03 | 0.020 | 1.000 | 2 | 2009 | 2019 | ||||
|
2 | 7 | 150947362 | missense variant | T/C | snv | 7.0E-06 | 0.020 | 1.000 | 2 | 2014 | 2018 | ||||||
|
70 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 0.020 | 1.000 | 2 | 2004 | 2011 | ||||
|
4 | 0.925 | 0.120 | 4 | 113348277 | missense variant | A/G | snv | 5.5E-04 | 8.3E-04 | 0.020 | 1.000 | 2 | 2003 | 2007 | |||
|
3 | 0.925 | 0.120 | 3 | 8745701 | missense variant | T/G | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
3 | 1.000 | 5 | 173232776 | stop gained | A/C;T | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||
|
5 | 0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
48 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
73 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
9 | 0.776 | 0.160 | 15 | 63060899 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 0.010 | 1.000 | 1 | 2004 | 2004 | |||
|
1 | 11 | 2776007 | synonymous variant | G/A | snv | 0.21 | 0.16 | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||
|
44 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.925 | 0.120 | 11 | 2572984 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
2 | 1.000 | 0.120 | 4 | 113355900 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 0.010 | < 0.001 | 1 | 2004 | 2004 | |||
|
4 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||
|
3 | 0.925 | 0.120 | 1 | 237454396 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
3 | 0.925 | 0.080 | 1 | 237819181 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
3 | 0.925 | 0.040 | 12 | 54582053 | missense variant | C/T | snv | 2.7E-02 | 0.010 | 1.000 | 1 | 2015 | 2015 |