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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 8 | 55198762 | intron variant | A/C | snv | 0.20 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
2 | 8 | 19405853 | missense variant | A/C | snv | 1.5E-04 | 9.8E-05 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
14 | 0.776 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
|
19 | 0.724 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 4.0E-06; 0.32 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 1.000 | 0.080 | 10 | 130032376 | intron variant | A/C;T | snv | 0.21 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
5 | 1.000 | 2 | 194695273 | intergenic variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||
|
188 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 0.040 | 0.500 | 4 | 2006 | 2013 | |||
|
2 | 1.000 | 0.080 | 16 | 56639236 | intron variant | A/G | snv | 0.71 | 0.67 | 0.010 | 1.000 | 1 | 2008 | 2008 | |||
|
3 | 0.925 | 0.080 | 19 | 10819992 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
|
7 | 0.827 | 0.200 | 1 | 161306821 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
3 | 1.000 | 0.120 | 2 | 67075611 | intergenic variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
7 | 0.807 | 0.240 | 6 | 36026129 | upstream gene variant | A/G | snv | 0.14 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
4 | 0.882 | 0.080 | 8 | 74360194 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
16 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
2 | 1.000 | 0.040 | 3 | 158669595 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
1 | 15 | 101178712 | missense variant | A/G | snv | 1.2E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
5 | 1.000 | 13 | 93226778 | non coding transcript exon variant | A/G | snv | 3.7E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 1.000 | 3 | 66395177 | intron variant | A/G | snv | 5.2E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
214 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
223 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
4 | 0.882 | 0.080 | 19 | 40396207 | stop gained | A/T | snv | 8.0E-06 | 5.6E-05 | 0.010 | 1.000 | 1 | 2002 | 2002 | |||
|
4 | 0.882 | 0.080 | 1 | 10258602 | missense variant | A/T | snv | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||
|
3 | 0.925 | 0.040 | 7 | 76303007 | missense variant | C/A | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
5 | 1.000 | 13 | 106686453 | intron variant | C/A | snv | 0.62 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 0.851 | 0.120 | 16 | 1792338 | stop gained | C/A | snv | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 |