| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | 12 | 73596057 | intergenic variant | C/G | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.882 | 0.160 | 18 | 55997051 | non coding transcript exon variant | A/G | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.882 | 0.160 | 5 | 164462274 | intron variant | G/T | snv | 0.89 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.080 | 16 | 74438798 | intron variant | C/T | snv | 0.61 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.080 | 3 | 27145111 | intron variant | C/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.882 | 0.120 | 10 | 121586602 | intron variant | G/A | snv | 0.54 |
|
0.710 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.925 | 0.080 | 11 | 1920716 | intron variant | T/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.807 | 0.240 | 17 | 50196930 | intron variant | T/A;G | snv |
|
0.710 | 0.500 | 1 | 2007 | 2011 | |||||||||
|
0.851 | 0.120 | 2 | 212432139 | intron variant | T/C | snv | 0.10 |
|
0.710 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.160 | 6 | 127279485 | intron variant | G/A | snv | 0.73 |
|
0.740 | 0.800 | 1 | 2008 | 2012 | ||||||||
|
0.851 | 0.080 | 20 | 34000289 | intron variant | T/C;G | snv |
|
0.710 | < 0.001 | 1 | 2012 | 2012 | |||||||||
|
0.882 | 0.080 | 10 | 5844771 | upstream gene variant | C/T | snv | 0.47 |
|
0.720 | 1.000 | 1 | 2010 | 2012 | ||||||||
|
0.851 | 0.080 | 10 | 121573063 | intron variant | C/G;T | snv |
|
0.720 | 1.000 | 1 | 2009 | 2012 | |||||||||
|
0.807 | 0.320 | 14 | 68283210 | intron variant | G/A | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.080 | 3 | 150750021 | intron variant | G/T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.160 | 11 | 129603795 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.080 | 5 | 44874903 | regulatory region variant | A/C;T | snv |
|
0.710 | 1.000 | 1 | 2011 | 2012 | |||||||||
|
0.827 | 0.120 | 19 | 17282085 | missense variant | G/A | snv | 0.47 | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 1 | 84156830 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.080 | 10 | 112974337 | intron variant | A/C;G | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.080 | 15 | 77977130 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 4 | 121205653 | intron variant | G/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.080 | 4 | 121200339 | intron variant | A/G | snv | 4.8E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.080 | 1 | 204546897 | intron variant | A/G | snv | 0.65 | 0.57 |
|
0.810 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 6 | 10456473 | non coding transcript exon variant | C/A | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2013 | 2013 |