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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
12 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 0.040 | 1.000 | 4 | 2011 | 2019 | |||||
|
8 | 0.807 | 0.240 | 11 | 111908832 | missense variant | C/T | snv | 9.1E-04 | 8.7E-04 | 0.020 | 1.000 | 2 | 2010 | 2017 | |||
|
2 | 0.925 | 0.200 | 11 | 111910446 | missense variant | G/A;T | snv | 9.5E-05; 4.0E-06 | 6.3E-05 | 0.010 | 1.000 | 1 | 2020 | 2020 | |||
|
4 | 0.882 | 0.080 | 11 | 111908822 | missense variant | C/T | snv | 7.2E-05 | 4.9E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
3 | 0.925 | 0.200 | 11 | 111908781 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
2 | 0.925 | 0.040 | 11 | 111911691 | missense variant | G/A | snv | 2.3E-05 | 3.5E-05 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
5 | 0.827 | 0.200 | 11 | 111911559 | missense variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
4 | 0.882 | 0.280 | 11 | 111908967 | missense variant | C/A;G | snv | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||
|
3 | 0.882 | 0.040 | 11 | 111908925 | missense variant | G/A | snv | 2.0E-05 | 4.9E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
3 | 0.882 | 0.040 | 11 | 111911694 | missense variant | G/A;C | snv | 3.2E-05 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 11 | 111911693 | missense variant | C/T | snv | 1.8E-05 | 4.2E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 |