| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518934 | 0.851 | 0.240 | 15 | 28211095 | frameshift variant | G/- | delins | 8 | |||
| rs1555444543 | 15 | 28260816 | inframe deletion | GTCCAGTCCTGGCAA/- | del | 1 | |||||
| rs1057519727 | 15 | 28260829 | missense variant | A/G | snv | 1 | |||||
| rs752908306 | 15 | 28272372 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||||
| rs916977 | 1.000 | 0.080 | 15 | 28268218 | intron variant | T/C;G | snv | 1 | |||
| rs12913832 | 0.763 | 0.200 | 15 | 28120472 | intron variant | A/G | snv | 0.50 | 1 | ||
| rs1667394 | 15 | 28285036 | intron variant | C/A;T | snv | 1 | |||||
| rs1555415658 | 1.000 | 15 | 28175633 | stop gained | A/T | snv | 1 | ||||
| rs397518474 | 1.000 | 15 | 28265707 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |