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 | 6 | 139373341 | missense variant | G/T | snv | 1.6E-04 | 5.2E-04 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
2 | 0.925 | 0.080 | 7 | 144399832 | missense variant | C/T | snv | 3.4E-04 | 2.9E-04 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
3 | 0.882 | 0.080 | 7 | 144399847 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-04 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
77 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 0.020 | 1.000 | 2 | 2014 | 2015 | ||||
|
62 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 0.925 | 0.080 | 6 | 152007481 | intron variant | T/C | snv | 0.39 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
2 | 0.925 | 0.080 | 4 | 155197173 | intron variant | A/G | snv | 0.66 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
2 | 0.925 | 0.080 | 2 | 162147505 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 0.010 | < 0.001 | 1 | 2012 | 2012 | |||
|
2 | 0.925 | 0.080 | 5 | 176887433 | intron variant | C/T | snv | 0.36 | 0.29 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
2 | 0.925 | 0.080 | 1 | 183125412 | missense variant | T/C | snv | 0.58 | 0.51 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
1 | 1.000 | 0.040 | 3 | 189894239 | stop gained | C/A;T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 3 | 189894253 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.925 | 0.200 | 2 | 208442425 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 2 | 219575194 | missense variant | G/A | snv | 2.3E-02 | 1.7E-02 | 0.080 | 0.625 | 8 | 2002 | 2014 | |||
|
2 | 0.925 | 0.080 | 1 | 22129830 | synonymous variant | C/A;T | snv | 1.2E-05; 3.2E-05 | 0.010 | < 0.001 | 1 | 2012 | 2012 | ||||
|
144 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
2 | 0.925 | 0.080 | 3 | 30686798 | intron variant | G/C | snv | 0.14 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
2 | 0.925 | 0.080 | 22 | 32844303 | intron variant | A/G | snv | 0.69 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.080 | 6 | 32976646 | missense variant | G/A | snv | 4.1E-06 | 0.030 | 0.667 | 3 | 2006 | 2010 | ||||
|
2 | 0.925 | 0.080 | 6 | 32976773 | missense variant | T/C | snv | 8.1E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
4 | 0.851 | 0.120 | 6 | 32976868 | missense variant | G/A | snv | 4.1E-06 | 7.0E-06 | 0.020 | 1.000 | 2 | 2004 | 2007 | |||
|
2 | 0.925 | 0.080 | 7 | 33345650 | intron variant | G/C;T | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||
|
2 | 0.925 | 0.080 | 7 | 33349101 | missense variant | G/A | snv | 0.21 | 0.18 | 0.010 | 1.000 | 1 | 2008 | 2008 | |||
|
2 | 0.925 | 0.080 | 7 | 33384348 | intron variant | T/A | snv | 0.42 | 0.010 | 1.000 | 1 | 2008 | 2008 |