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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 0.882 | 0.120 | 8 | 1780316 | missense variant | C/T | snv | 3.2E-05 | 7.0E-06 | 0.700 | 1.000 | 4 | 2004 | 2014 | |||
|
3 | 0.882 | 0.120 | 8 | 1771124 | missense variant | C/G;T | snv | 1.0E-04; 2.4E-05 | 0.700 | 1.000 | 2 | 2000 | 2004 | ||||
|
2 | 0.925 | 0.120 | 8 | 1771553 | stop gained | G/C;T | snv | 8.0E-06; 1.2E-05 | 0.700 | 0 | |||||||
|
5 | 0.851 | 0.160 | 8 | 1780498 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 0 |