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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 0.830 | 1.000 | 32 | 1995 | 2017 | |||||
|
4 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 0.820 | 1.000 | 22 | 1995 | 2019 | |||||
|
1 | 1.000 | 0.120 | 7 | 150952574 | missense variant | T/C | snv | 0.810 | 1.000 | 25 | 1995 | 2017 | |||||
|
6 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 0.810 | 1.000 | 21 | 1995 | 2014 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951738 | missense variant | A/G | snv | 7.2E-05 | 5.6E-05 | 0.800 | 1.000 | 29 | 1995 | 2017 | |||
|
1 | 1.000 | 0.120 | 7 | 150952630 | missense variant | G/A | snv | 2.4E-05 | 1.4E-05 | 0.800 | 1.000 | 25 | 1995 | 2017 | |||
|
3 | 0.882 | 0.120 | 7 | 150951552 | missense variant | G/A | snv | 0.800 | 1.000 | 25 | 1995 | 2009 | |||||
|
2 | 0.925 | 0.120 | 7 | 150948939 | missense variant | C/A;T | snv | 0.800 | 1.000 | 25 | 1995 | 2017 | |||||
|
3 | 0.882 | 0.120 | 7 | 150950311 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.800 | 1.000 | 24 | 1995 | 2017 | |||
|
1 | 1.000 | 0.120 | 7 | 150974926 | missense variant | A/C;G;T | snv | 0.800 | 1.000 | 24 | 1995 | 2017 | |||||
|
1 | 1.000 | 0.120 | 7 | 150952744 | missense variant | A/C;G | snv | 0.800 | 1.000 | 24 | 1995 | 2017 | |||||
|
1 | 1.000 | 0.120 | 7 | 150951517 | missense variant | C/T | snv | 0.800 | 1.000 | 24 | 1995 | 2017 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951507 | missense variant | T/A;C;G | snv | 0.800 | 1.000 | 24 | 1995 | 2017 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951505 | missense variant | C/G;T | snv | 2.0E-05 | 0.800 | 1.000 | 24 | 1995 | 2017 | ||||
|
2 | 0.925 | 0.120 | 7 | 150948938 | missense variant | T/C | snv | 0.800 | 1.000 | 24 | 1995 | 2017 | |||||
|
4 | 0.851 | 0.120 | 7 | 150951643 | missense variant | C/A;G;T | snv | 8.0E-06 | 0.800 | 1.000 | 24 | 1995 | 2012 | ||||
|
1 | 1.000 | 0.120 | 7 | 150950246 | missense variant | C/A | snv | 0.800 | 1.000 | 23 | 1995 | 2012 | |||||
|
3 | 0.882 | 0.120 | 7 | 150958449 | missense variant | G/A;C | snv | 3.2E-04 | 0.800 | 1.000 | 23 | 1995 | 2012 | ||||
|
1 | 1.000 | 0.120 | 7 | 150951473 | missense variant | G/C;T | snv | 0.800 | 1.000 | 21 | 1995 | 2016 | |||||
|
2 | 0.925 | 0.120 | 7 | 150948984 | missense variant | C/G;T | snv | 0.800 | 1.000 | 20 | 1995 | 2009 | |||||
|
2 | 0.925 | 0.120 | 7 | 150951649 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1995 | 2009 | |||||
|
2 | 0.925 | 0.120 | 7 | 150948995 | missense variant | G/A | snv | 4.0E-06 | 0.800 | 1.000 | 20 | 1995 | 2009 | ||||
|
2 | 0.925 | 0.120 | 7 | 150974825 | missense variant | T/G | snv | 0.800 | 1.000 | 20 | 1995 | 2009 | |||||
|
1 | 1.000 | 0.120 | 7 | 150948866 | missense variant | T/A;C;G | snv | 0.800 | 1.000 | 20 | 1995 | 2009 | |||||
|
3 | 0.882 | 0.120 | 7 | 150951721 | missense variant | C/G | snv | 0.800 | 1.000 | 20 | 1995 | 2009 |