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 | 0.040 | 10 | 87864514 | missense variant | A/C;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 10 | 87894052 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 10 | 87925518 | stop gained | T/A;G | snv | 0.700 | 0 | ||||||||
|
12 | 0.752 | 0.200 | 10 | 87933144 | stop gained | G/A;T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 |