| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3800316 | 1.000 | 0.040 | 6 | 27288323 | intron variant | A/C | snv | 0.33 | 1 | ||
| rs3800318 | 1.000 | 0.040 | 6 | 27295862 | intron variant | A/T | snv | 0.18 | 1 | ||
| rs7746199 | 1.000 | 0.040 | 6 | 27293545 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs16897515 | 1.000 | 0.040 | 6 | 27310241 | missense variant | C/A | snv | 0.13 | 0.18 | 1 |