| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28928910 | 0.827 | 0.200 | 8 | 24956452 | missense variant | G/A;T | snv | 11 | |||
| rs58982919 | 0.790 | 0.080 | 8 | 24956223 | missense variant | T/C | snv | 10 | |||
| rs57105105 | 0.925 | 0.080 | 8 | 24953776 | missense variant | C/T | snv | 4 | |||
| rs60261494 | 0.882 | 0.080 | 8 | 24956493 | missense variant | GG/CT | mnv | 3 | |||
| rs62636503 | 0.882 | 0.080 | 8 | 24953779 | missense variant | C/T | snv | 3 | |||
| rs62636505 | 0.925 | 0.080 | 8 | 24956235 | missense variant | A/G | snv | 2 | |||
| rs59443585 | 0.925 | 0.080 | 8 | 24955521 | missense variant | T/G | snv | 2 | |||
| rs587777881 | 1.000 | 0.080 | 8 | 24955509 | missense variant | A/G | snv | 1 | |||
| rs587777882 | 1.000 | 0.080 | 8 | 24953646 | missense variant | G/A;C | snv | 1 | |||
| rs757417962 | 1.000 | 0.080 | 8 | 24954233 | stop gained | G/A;C | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs58640772 | 1.000 | 0.080 | 8 | 24956455 | frameshift variant | -/TCCACGTAGCGCC | delins | 1 | |||
| rs876661155 | 1.000 | 0.080 | 8 | 24956029 | stop gained | C/A;G | snv | 1 | |||
| rs1411999109 | 1.000 | 0.080 | 8 | 24955720 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs191346286 | 1.000 | 0.080 | 8 | 24953704 | stop gained | G/A;T | snv | 4.4E-05 | 1 | ||
| rs587777880 | 1.000 | 0.080 | 8 | 24955722 | missense variant | T/C | snv | 1 | |||
| rs62636502 | 1.000 | 0.080 | 8 | 24955713 | missense variant | A/C;G | snv | 1 |