| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs200564757 | 0.925 | 0.080 | 15 | 67236060 | stop gained | G/A;T | snv | 2.0E-05 | 2 | ||
| rs746488412 | 0.925 | 0.080 | 15 | 67231868 | stop gained | G/A | snv | 8.0E-06 | 2 | ||
| rs1057518846 | 1.000 | 0.080 | 15 | 67235978 | splice donor variant | C/A;G | snv | 1 | |||
| rs1254374766 | 1.000 | 0.080 | 15 | 67208580 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs1567027297 | 1.000 | 0.080 | 15 | 67236420 | frameshift variant | CT/- | delins | 1 | |||
| rs1567027610 | 1.000 | 0.080 | 15 | 67236690 | frameshift variant | GAAA/- | delins | 1 | |||
| rs7173826 | 15 | 67236036 | missense variant | T/C;G | snv | 8.0E-06; 0.37 | 1 | ||||
| rs753247583 | 1.000 | 0.080 | 15 | 67203547 | splice donor variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs781596375 | 1.000 | 0.080 | 15 | 67231876 | frameshift variant | C/- | delins | 1 | |||
| rs3743347 | 15 | 67254963 | intron variant | C/A;T | snv | 0.26; 8.2E-06 | 1 |