| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs747229909 | 1.000 | 0.120 | 15 | 68211716 | missense variant | G/A;C | snv | 5.6E-05 | 1 | ||
| rs774543080 | 0.925 | 0.120 | 15 | 68211765 | frameshift variant | AG/- | delins | 8.0E-06 | 2 | ||
| rs104894484 | 1.000 | 0.120 | 15 | 68211793 | missense variant | C/T | snv | 1 | |||
| rs397515352 | 0.925 | 0.120 | 15 | 68211844 | frameshift variant | -/G | delins | 2.4E-05; 2.8E-05 | 3 | ||
| rs553192210 | 1.000 | 0.120 | 15 | 68214177 | non coding transcript exon variant | C/A;G | snv | 2.8E-05 | 1 | ||
| rs786205067 | 1.000 | 0.120 | 15 | 68214315 | frameshift variant | -/CGTT | delins | 1 | |||
| rs1567096598 | 1.000 | 0.120 | 15 | 68214337 | missense variant | A/T | snv | 1 | |||
| rs104894483 | 0.925 | 0.120 | 15 | 68214373 | stop gained | C/A;G;T | snv | 6.8E-05; 2.6E-03; 2.0E-05; 4.0E-06 | 3 | ||
| rs154774633 | 0.925 | 0.120 | 15 | 68214387 | missense variant | A/G | snv | 2 | |||
| rs751486476 | 0.925 | 0.160 | 15 | 68218549 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs154774640 | 0.925 | 0.120 | 15 | 68218584 | stop gained | G/C | snv | 8.0E-06 | 2.1E-05 | 2 | |
| rs1555440188 | 1.000 | 0.120 | 15 | 68229500 | splice donor variant | A/C | snv | 1 | |||
| rs1381427322 | 1.000 | 0.120 | 15 | 68229502 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
| rs763944821 | 1.000 | 0.120 | 15 | 68229536 | missense variant | C/T | snv | 8.2E-04 | 9.8E-05 | 1 | |
| rs154774636 | 0.925 | 0.120 | 15 | 68229568 | missense variant | C/G | snv | 2 | |||
| rs786205065 | 1.000 | 0.120 | 15 | 68229578 | frameshift variant | C/- | delins | 1 | |||
| rs1555440206 | 1.000 | 0.120 | 15 | 68229584 | start lost | T/C | snv | 1 |