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 | 0.925 | 0.080 | 11 | 101504634 | missense variant | G/T | snv | 0.800 | 1.000 | 11 | 2005 | 2016 | |||||
|
1 | 1.000 | 0.080 | 11 | 101504541 | missense variant | T/C | snv | 4.8E-05 | 1.7E-04 | 0.800 | 1.000 | 11 | 2005 | 2016 | |||
|
1 | 1.000 | 0.080 | 11 | 101504161 | missense variant | A/T | snv | 0.800 | 1.000 | 11 | 2005 | 2016 | |||||
|
1 | 1.000 | 0.080 | 11 | 101453068 | missense variant | G/A | snv | 0.800 | 1.000 | 11 | 2005 | 2016 | |||||
|
2 | 0.925 | 0.080 | 11 | 101453062 | missense variant | C/T | snv | 0.800 | 1.000 | 11 | 2005 | 2016 | |||||
|
3 | 0.882 | 0.080 | 11 | 101504595 | missense variant | T/C | snv | 2.0E-04 | 2.2E-04 | 0.700 | 1.000 | 11 | 2005 | 2016 | |||
|
1 | 1.000 | 0.080 | 11 | 101491605 | missense variant | C/T | snv | 3.2E-05 | 2.1E-05 | 0.700 | 1.000 | 11 | 2005 | 2016 | |||
|
3 | 0.882 | 0.080 | 11 | 101504316 | missense variant | T/A | snv | 1.2E-05 | 1.4E-05 | 0.700 | 1.000 | 11 | 2005 | 2016 | |||
|
1 | 1.000 | 0.080 | 11 | 101504445 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 11 | 101504451 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 11 | 101471253 | missense variant | A/G | snv | 2.0E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 11 | 101453674 | stop gained | T/A | snv | 0.700 | 0 |