| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893950 | 0.925 | 0.080 | 6 | 145627691 | stop gained | G/A;C | snv | 7.7E-05 | 2 | ||
| rs201053542 | 1.000 | 0.080 | 6 | 145627618 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs137852917 | 1.000 | 0.080 | 6 | 145627577 | missense variant | C/A;T | snv | 8.0E-06; 1.2E-05 | 1 | ||
| rs796052427 | 1.000 | 0.080 | 6 | 145627534 | missense variant | T/A | snv | 1 | |||
| rs796052428 | 1.000 | 0.080 | 6 | 145627510 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs587776554 | 1.000 | 0.080 | 6 | 145627458 | frameshift variant | -/A | delins | 1 | |||
| rs387907571 | 0.827 | 0.080 | 3 | 132477995 | missense variant | A/G | snv | 4.2E-06 | 3.5E-05 | 6 |