| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs794726860 | 0.925 | 3 | 11025786 | missense variant | C/T | snv | 3 | ||||
| rs876657400 | 0.925 | 0.080 | 3 | 11025812 | missense variant | G/A | snv | 2 | |||
| rs1064795099 | 1.000 | 3 | 11031230 | missense variant | C/A;G | snv | 1 | ||||
| rs1553688970 | 1.000 | 3 | 11022385 | frameshift variant | CTGGCCATCACGCTGGCCA/- | delins | 1 | ||||
| rs1553689859 | 1.000 | 3 | 11026351 | missense variant | C/T | snv | 1 | ||||
| rs1553690583 | 1.000 | 3 | 11029283 | frameshift variant | C/- | delins | 1 | ||||
| rs1553691674 | 1.000 | 3 | 11033638 | splice acceptor variant | G/A;T | snv | 1 | ||||
| rs1559639240 | 1.000 | 3 | 11033672 | missense variant | T/C | snv | 1 | ||||
| rs745529755 | 1.000 | 3 | 11033647 | stop gained | C/A;T | snv | 1.2E-05 | 7.0E-06 | 1 | ||
| rs749240316 | 1.000 | 3 | 11026281 | missense variant | G/A;C | snv | 4.0E-06 | 1 | |||
| rs876657401 | 1.000 | 3 | 11031222 | frameshift variant | GG/- | del | 1 | ||||
| rs886042046 | 1.000 | 3 | 11034651 | missense variant | G/A;C | snv | 1 | ||||
| rs1064795852 | 1.000 | 3 | 11017434 | missense variant | G/A | snv | 1 | ||||
| rs794726859 | 1.000 | 3 | 11017342 | missense variant | G/A;C | snv | 1 | ||||
| rs1064795290 | 1.000 | 3 | 11017921 | missense variant | A/G | snv | 1 | ||||
| rs1559623389 | 1.000 | 3 | 11018699 | splice donor variant | G/T | snv | 1 |