| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854435 | 0.925 | 0.080 | 8 | 143728488 | stop gained | G/A | snv | 2 | |||
| rs137854436 | 0.925 | 0.080 | 8 | 143728269 | stop gained | G/A | snv | 2 | |||
| rs137854438 | 1.000 | 0.080 | 8 | 143728570 | stop gained | A/T | snv | 2 | |||
| rs137854437 | 1.000 | 0.080 | 8 | 143728218 | stop gained | C/A;T | snv | 1.4E-05 | 1 | ||
| rs137854439 | 1.000 | 0.080 | 8 | 143728081 | stop gained | C/G;T | snv | 4.2E-06 | 1 | ||
| rs137854440 | 1.000 | 0.080 | 8 | 143727432 | stop gained | G/A | snv | 1 | |||
| rs137854441 | 1.000 | 0.080 | 8 | 143728053 | stop gained | G/A | snv | 1 | |||
| rs137854442 | 1.000 | 0.080 | 8 | 143728601 | stop gained | G/A;T | snv | 2.1E-05 | 1 | ||
| rs137854444 | 1.000 | 0.080 | 8 | 143728082 | stop gained | C/T | snv | 1 | |||
| rs1554623490 | 1.000 | 0.080 | 8 | 143728534 | frameshift variant | AC/- | delins | 1 | |||
| rs312262803 | 1.000 | 0.080 | 8 | 143727792 | missense variant | C/A | snv | 6.4E-03 | 1.8E-03 | 1 | |
| rs387907056 | 1.000 | 0.080 | 8 | 143728095 | stop gained | G/A;C | snv | 1 | |||
| rs796065023 | 1.000 | 0.080 | 8 | 143728537 | frameshift variant | AG/- | delins | 1 |