| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1567262537 | 1.000 | 0.120 | 16 | 3729142 | stop gained | G/A | snv | 1 | |||
| rs1567269316 | 1.000 | 0.120 | 16 | 3736104 | stop gained | T/A | snv | 1 | |||
| rs1567277287 | 1.000 | 0.120 | 16 | 3745356 | splice acceptor variant | T/A | snv | 1 | |||
| rs1567287477 | 1.000 | 0.120 | 16 | 3757906 | missense variant | G/C | snv | 1 | |||
| rs1567309482 | 1.000 | 0.120 | 16 | 3782694 | frameshift variant | AG/- | delins | 1 | |||
| rs1567316655 | 1.000 | 0.120 | 16 | 3792030 | frameshift variant | CA/- | delins | 1 | |||
| rs1567318022 | 1.000 | 0.120 | 16 | 3793539 | frameshift variant | -/T | delins | 1 | |||
| rs28937315 | 1.000 | 0.120 | 16 | 3757894 | missense variant | T/C | snv | 1 | |||
| rs886041048 | 1.000 | 0.120 | 16 | 3739725 | splice acceptor variant | C/A | snv | 1 | |||
| rs886041286 | 1.000 | 0.120 | 16 | 3736771 | missense variant | T/C | snv | 1 | |||
| rs1555910114 | 1.000 | 0.120 | 22 | 41157167 | splice acceptor variant | A/G | snv | 1 |