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 | 11 | 77183146 | missense variant | C/A;T | snv | 3.9E-05 | 1.5E-04 | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.200 | 17 | 74920325 | stop gained | C/A;T | snv | 4.1E-06; 8.1E-06 | 0.700 | 0 | |||||||
|
1 | 2 | 178454526 | stop gained | C/T | snv | 1.6E-05 | 1.4E-05 | 0.700 | 0 | ||||||||
|
1 | 2 | 178453567 | stop gained | C/G;T | snv | 4.0E-06 | 0.700 | 0 | |||||||||
|
2 | 1.000 | 21 | 36461442 | missense variant | A/G;T | snv | 4.0E-06; 2.0E-05 | 0.700 | 0 | ||||||||
|
1 | 11 | 77205503 | missense variant | C/G;T | snv | 6.4E-05 | 2.1E-05 | 0.700 | 0 | ||||||||
|
1 | 11 | 77204094 | missense variant | G/A;C | snv | 8.8E-06; 4.4E-05 | 0.700 | 0 | |||||||||
|
1 | 1 | 108896945 | missense variant | C/A | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||||
|
1 | 9 | 72816175 | missense variant | C/G;T | snv | 1.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||||
|
1 | 10 | 71791284 | missense variant | A/C | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||||
|
1 | 1 | 216199777 | stop gained | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||||
|
1 | 9 | 72789302 | stop gained | G/A;C | snv | 4.0E-06 | 0.700 | 0 |