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 | 0.925 | 0.160 | 2 | 47416351 | missense variant | G/A | snv | 0.800 | 1.000 | 0 | 2003 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47475244 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47466702 | missense variant | T/A;C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.882 | 0.160 | 2 | 47429833 | missense variant | C/G;T | snv | 1.5E-03 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.160 | 2 | 47478337 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47429819 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.160 | 2 | 47478498 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.160 | 2 | 47412414 | missense variant | A/C;G;T | snv | 4.0E-06; 8.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.160 | 2 | 47410212 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47476529 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47408482 | missense variant | A/G;T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.160 | 2 | 47470988 | missense variant | A/T | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.160 | 2 | 47476502 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.160 | 2 | 47476372 | missense variant | A/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 0.882 | 0.160 | 2 | 47475064 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47410251 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 0.925 | 0.160 | 2 | 47410287 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 2 | 47414389 | missense variant | G/A | snv | 6.0E-05 | 7.9E-05 | 0.700 | 0 | ||||||
|
1 | 0.851 | 0.240 | 2 | 47466718 | missense variant | G/A;C;T | snv | 8.0E-06 | 0.800 | 1.000 | 14 | 2001 | 2017 | ||||
|
1 | 1.000 | 0.160 | 2 | 47466801 | missense variant | A/C;G | snv | 0.700 | 1.000 | 14 | 2001 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47412504 | stop gained | A/C;G;T | snv | 0.700 | 1.000 | 14 | 2001 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47476450 | missense variant | T/C | snv | 0.700 | 1.000 | 14 | 2001 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47408466 | missense variant | C/T | snv | 0.700 | 1.000 | 14 | 2001 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47478306 | stop gained | G/A;T | snv | 0.700 | 1.000 | 14 | 2001 | 2017 | |||||
|
1 | 0.925 | 0.160 | 2 | 47429742 | missense variant | A/T | snv | 0.700 | 1.000 | 14 | 2001 | 2017 |