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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 1.000 | 0.080 | 3 | 9684627 | missense variant | G/A | snv | 8.0E-06 | 0.700 | 1.000 | 1 | 2006 | 2006 | ||||
|
2 | 1.000 | 0.080 | 3 | 9689034 | missense variant | A/G | snv | 8.0E-06 | 2.1E-05 | 0.700 | 1.000 | 1 | 2006 | 2006 | |||
|
2 | 0.925 | 0.120 | 19 | 10823859 | missense variant | C/A | snv | 0.700 | 1.000 | 9 | 2005 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 10812273 | missense variant | A/C;G | snv | 0.700 | 1.000 | 9 | 2005 | 2012 | |||||
|
2 | 0.925 | 0.080 | 19 | 10823868 | missense variant | T/C | snv | 0.700 | 1.000 | 9 | 2005 | 2012 | |||||
|
2 | 0.925 | 0.080 | 19 | 10823886 | missense variant | C/G | snv | 0.700 | 1.000 | 9 | 2005 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 10819986 | missense variant | G/A | snv | 0.700 | 1.000 | 9 | 2005 | 2012 | |||||
|
3 | 0.882 | 0.120 | 19 | 10793833 | missense variant | G/A;T | snv | 0.800 | 1.000 | 10 | 2005 | 2012 | |||||
|
3 | 0.882 | 0.120 | 19 | 10793832 | missense variant | C/T | snv | 7.0E-06 | 0.800 | 1.000 | 10 | 2005 | 2012 | ||||
|
4 | 0.882 | 0.120 | 19 | 10793829 | missense variant | G/A | snv | 0.800 | 1.000 | 10 | 2005 | 2012 | |||||
|
3 | 0.882 | 0.120 | 19 | 10823862 | missense variant | C/G;T | snv | 0.800 | 1.000 | 10 | 2005 | 2012 | |||||
|
3 | 0.882 | 0.120 | 19 | 10812271 | missense variant | G/A;T | snv | 0.800 | 1.000 | 11 | 2005 | 2012 | |||||
|
4 | 0.851 | 0.120 | 19 | 10798543 | missense variant | C/T | snv | 0.800 | 1.000 | 13 | 2005 | 2016 |