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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 5 | 1994 | 2011 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.010 | < 0.001 | 1 | 2001 | 2001 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.010 | < 0.001 | 1 | 2001 | 2001 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.010 | < 0.001 | 1 | 2001 | 2001 | |||||||||
|
0.701 | 0.280 | 17 | 7675125 | missense variant | A/C;G;T | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 |