| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
| rs988748 | 0.882 | 0.120 | 11 | 27703198 | intron variant | C/G | snv | 0.83 | 3 | ||
| rs11644461 | 1.000 | 0.080 | 16 | 10027033 | intron variant | T/C | snv | 0.34 | 1 | ||
| rs7192557 | 1.000 | 0.080 | 16 | 10029612 | intron variant | G/A;T | snv | 0.21 | 1 |