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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.120 | X | 103788460 | missense variant | C/T | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103787831 | missense variant | T/C | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103787811 | missense variant | C/G;T | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103788469 | missense variant | G/T | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103787888 | missense variant | A/C | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103788485 | missense variant | T/C | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103787951 | missense variant | G/A;C | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103786493 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103785705 | missense variant | C/T | snv | 0.800 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 0.925 | 0.120 | X | 103788475 | missense variant | G/T | snv | 0.700 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103788497 | missense variant | G/A | snv | 0.700 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 0.925 | 0.120 | X | 103789373 | missense variant | G/C | snv | 0.700 | 1.000 | 20 | 1989 | 2000 | |||||
|
1 | 1.000 | 0.120 | X | 103785675 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | X | 103789375 | missense variant | G/A | snv | 0.700 | 0 |