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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 0.732 | 0.160 | 10 | 43113649 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 12 | 1996 | 2015 | |||||
|
4 | 0.776 | 0.200 | 10 | 43113654 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 8 | 1994 | 2015 | |||||
|
2 | 0.790 | 0.280 | 10 | 43113628 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 6 | 1996 | 2017 | |||||
|
4 | 0.807 | 0.160 | 10 | 43118458 | missense variant | G/C;T | snv | 4.0E-06; 2.0E-05 | 0.700 | 1.000 | 16 | 1998 | 2018 | ||||
|
11 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 0.700 | 1.000 | 8 | 1994 | 2015 | ||||
|
9 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 0.700 | 1.000 | 7 | 1994 | 2016 | ||||
|
10 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 0.700 | 1.000 | 9 | 1994 | 2017 | ||||
|
2 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 0.700 | 1.000 | 7 | 1995 | 2012 | ||||
|
14 | 0.662 | 0.360 | 10 | 43119548 | missense variant | G/A;C;T | snv | 1.2E-04; 4.3E-06 | 0.700 | 1.000 | 19 | 1995 | 2016 | ||||
|
3 | 0.851 | 0.120 | 10 | 43114596 | missense variant | A/C;G | snv | 8.0E-06 | 0.700 | 1.000 | 3 | 2005 | 2015 | ||||
|
9 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 0.700 | 1.000 | 11 | 1994 | 2017 | ||||
|
3 | 0.827 | 0.160 | 10 | 43113656 | missense variant | C/G;T | snv | 1.6E-05 | 0.700 | 1.000 | 7 | 1997 | 2015 | ||||
|
3 | 0.807 | 0.120 | 10 | 43114598 | missense variant | G/C;T | snv | 2.4E-05 | 0.700 | 1.000 | 11 | 2005 | 2016 |