| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs696 | 0.708 | 0.520 | 14 | 35401887 | 3 prime UTR variant | C/T | snv | 0.45 | 22 | ||
| rs753482595 | 0.925 | 0.200 | 4 | 9920389 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 3 | |
| rs767816037 | 1.000 | 0.080 | 17 | 63872725 | missense variant | C/G;T | snv | 4.5E-05 | 1 | ||
| rs775020499 | 1.000 | 0.080 | 9 | 127467764 | missense variant | A/G | snv | 8.2E-06 | 1 | ||
| rs782818582 | 0.882 | 0.160 | 9 | 133456116 | stop gained | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs8094315 | 1.000 | 0.080 | 18 | 63268814 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs9617814 | 1.000 | 0.080 | 22 | 19622420 | regulatory region variant | A/G | snv | 0.22 | 1 |