| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762236241 | 0.882 | 0.080 | 17 | 75757312 | splice donor variant | T/C | snv | 2.0E-05 | 3 | ||
| rs80338755 | 0.925 | 0.080 | 17 | 75727423 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 2 | |
| rs121912464 | 1.000 | 0.080 | 17 | 75755785 | stop gained | G/A | snv | 1 | |||
| rs1559159868 | 1.000 | 0.080 | 2 | 172501823 | frameshift variant | A/- | delins | 1 | |||
| rs121912461 | 1.000 | 0.080 | 17 | 75727853 | missense variant | T/C | snv | 1 | |||
| rs121912462 | 1.000 | 0.080 | 17 | 75736053 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
| rs121912463 | 1.000 | 0.080 | 17 | 75736077 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs121912465 | 1.000 | 0.080 | 17 | 75727227 | missense variant | T/C | snv | 1 | |||
| rs121912468 | 1.000 | 0.080 | 17 | 75750992 | missense variant | G/A;T | snv | 1 | |||
| rs1304888529 | 1.000 | 0.080 | 17 | 75730476 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1422797135 | 1.000 | 0.080 | 17 | 75730349 | missense variant | C/T | snv | 1 | |||
| rs147222357 | 1.000 | 0.080 | 17 | 75751112 | splice donor variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs1476568580 | 1.000 | 0.080 | 17 | 75730320 | missense variant | G/A | snv | 4.0E-06 | 3.5E-05 | 1 | |
| rs201494421 | 1.000 | 0.080 | 17 | 75730256 | missense variant | C/G;T | snv | 8.1E-06 | 1 | ||
| rs772142634 | 1.000 | 0.080 | 17 | 75743736 | stop gained | C/T | snv | 8.0E-06 | 1 | ||
| rs121912467 | 1.000 | 0.080 | 17 | 75752221 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs794726676 | 1.000 | 0.080 | 17 | 75755759 | frameshift variant | G/- | delins | 1 |