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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
56 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 0.820 | 1.000 | 12 | 2008 | 2019 | ||||
|
4 | 0.882 | 0.160 | 4 | 88169725 | intron variant | T/C;G | snv | 0.800 | 1.000 | 4 | 2010 | 2015 | |||||
|
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 | |||||
|
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 | 10125817 | intergenic variant | T/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10080532 | intron variant | C/A;T | snv | 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 | 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 | 10044203 | intron variant | A/G;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10132824 | intergenic variant | G/A;C;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
5 | 0.925 | 0.120 | 6 | 25975655 | intron variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
4 | 0.925 | 0.120 | 6 | 25870314 | intron variant | T/A;G | snv | 0.700 | 1.000 | 3 | 2008 | 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 | 6 | 25858476 | intron variant | G/C;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10130513 | intergenic variant | G/A;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10128881 | intergenic variant | C/A;G | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 88109689 | intron variant | T/C;G | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10146951 | upstream gene variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 10147047 | upstream gene variant | G/A;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9971255 | intron variant | T/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9980567 | intron variant | C/G;T | snv | 0.47 | 0.700 | 1.000 | 3 | 2010 | 2013 | ||||
|
3 | 0.925 | 0.120 | 4 | 9980265 | intron variant | T/C;G | snv | 0.700 | 1.000 | 3 | 2010 | 2013 | |||||
|
3 | 0.925 | 0.120 | 4 | 9980373 | intron variant | G/A;T | snv | 0.700 | 1.000 | 3 | 2010 | 2013 |