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 | 0.040 | 20 | 49374576 | stop gained | G/A;C | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 20 | 49374416 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 20 | 49374559 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
6 | 1.000 | 0.040 | 20 | 49374625 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.040 | 20 | 49374644 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.040 | 20 | 49374931 | missense variant | G/A;C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49482353 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374312 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374359 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374380 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374421 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374428 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374430 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374455 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374515 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374592 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 49374703 | frameshift variant | A/- | del | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.040 | 20 | 49374519 | missense variant | G/C;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 20 | 49374377 | missense variant | C/T | snv | 0.700 | 0 |