| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs756632799 | 0.882 | 0.080 | 20 | 45416579 | stop gained | G/T | snv | 1.6E-05 | 7.0E-06 | 5 | |
| rs527236031 | 0.882 | 0.080 | 20 | 45424323 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 5 | |
| rs1277383877 | 0.925 | 20 | 45421428 | missense variant | G/T | snv | 7.0E-06 | 3 | |||
| rs774753616 | 1.000 | 20 | 45419351 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 3 | ||
| rs763009552 | 1.000 | 20 | 45416213 | frameshift variant | C/- | del | 1 | ||||
| rs527236032 | 1.000 | 20 | 45420578 | frameshift variant | -/T | ins | 1 | ||||
| rs571714796 | 1.000 | 20 | 45421445 | missense variant | G/A;T | snv | 4.0E-06 | 1 | |||
| rs751861982 | 1.000 | 20 | 45420577 | frameshift variant | -/C | delins | 3.6E-05 | 4.9E-05 | 1 | ||
| rs771157170 | 1.000 | 20 | 45425671 | missense variant | G/A;T | snv | 9.9E-05 | 1 | |||
| rs200790673 | 1.000 | 20 | 45419293 | splice acceptor variant | A/G | snv | 5.2E-05 | 6.3E-05 | 1 | ||
| rs587777027 | 1.000 | 20 | 45419348 | missense variant | A/C;G | snv | 1 |