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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.827 | 0.280 | 4 | 10000237 | intron variant | G/A | snv | 0.72 | 0.810 | 1.000 | 6 | 2010 | 2019 | ||||
|
4 | 0.882 | 0.160 | 4 | 9993558 | intron variant | G/A;C | snv | 0.800 | 1.000 | 4 | 2010 | 2016 | |||||
|
7 | 0.851 | 0.240 | 4 | 9921380 | intron variant | G/A;T | snv | 0.800 | 1.000 | 4 | 2010 | 2013 | |||||
|
5 | 0.925 | 0.120 | 4 | 9925343 | intron variant | T/G | snv | 0.39 | 0.800 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9945032 | intron variant | C/A | snv | 0.29 | 0.800 | 1.000 | 3 | 2010 | 2013 | ||||
|
7 | 0.827 | 0.200 | 4 | 9920543 | missense variant | C/T | snv | 0.24 | 0.29 | 0.710 | 1.000 | 5 | 2008 | 2016 | |||
|
5 | 0.925 | 0.120 | 4 | 9964756 | intron variant | A/G | snv | 0.28 | 0.700 | 1.000 | 5 | 2008 | 2013 | ||||
|
7 | 0.851 | 0.200 | 4 | 9934286 | intron variant | A/G | snv | 0.33 | 0.700 | 1.000 | 4 | 2007 | 2013 | ||||
|
7 | 0.851 | 0.240 | 4 | 9933120 | intron variant | G/A;T | snv | 0.700 | 1.000 | 4 | 2008 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9982851 | intron variant | C/T | snv | 0.21 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 10034516 | non coding transcript exon variant | C/A | snv | 0.78 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 10004913 | intron variant | C/A | snv | 0.72 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 10003208 | intron variant | A/G | snv | 0.72 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9983382 | intron variant | C/T | snv | 0.20 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9973014 | intron variant | A/G;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9949597 | intron variant | T/C | snv | 0.51 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9918723 | intron variant | T/C | snv | 0.51 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9996816 | synonymous variant | C/G;T | snv | 1.2E-05; 0.70 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 10036004 | non coding transcript exon variant | T/C | snv | 0.43 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 10044203 | intron variant | A/G;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9945654 | intron variant | T/C | snv | 0.57 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
6 | 0.851 | 0.160 | 4 | 9914117 | intron variant | C/T | snv | 0.32 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9979073 | intron variant | C/A;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10033830 | intron variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9950195 | intron variant | C/T | snv | 0.17 | 0.700 | 1.000 | 3 | 2010 | 2013 |