| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs864321670 | 0.763 | 0.320 | 10 | 95633012 | missense variant | C/T | snv | 24 | |||
| rs1014959895 | 0.763 | 0.360 | 16 | 68329105 | stop gained | G/C;T | snv | 4.0E-06; 1.6E-05 | 16 | ||
| rs1251713297 | 0.776 | 0.360 | 16 | 68355785 | stop gained | C/A | snv | 8.1E-06 | 15 | ||
| rs864309488 | 0.776 | 0.440 | 6 | 24777296 | missense variant | A/G | snv | 14 | |||
| rs878853220 | 0.827 | 0.200 | 1 | 156130818 | intron variant | T/G | snv | 6 | |||
| rs1554236040 | 0.882 | 0.320 | 6 | 157201464 | stop gained | C/T | snv | 5 | |||
| rs1554438441 | 0.882 | 0.040 | 7 | 143342006 | frameshift variant | -/TC | delins | 5 | |||
| rs1057519335 | 0.925 | 0.040 | 9 | 35792968 | missense variant | T/A | snv | 5 |