| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs772527880 | 2 | 227531108 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
| rs774847933 | 0.882 | 0.200 | 22 | 19962797 | missense variant | A/G | snv | 8.0E-06 | 5 | ||
| rs796065354 | 0.882 | 0.080 | 6 | 151944320 | missense variant | A/G | snv | 9 | |||
| rs9444584 | 0.882 | 0.160 | 6 | 88152840 | intron variant | C/T | snv | 0.30 | 4 | ||
| rs9450898 | 0.925 | 0.160 | 6 | 88154344 | intron variant | C/T | snv | 0.21 | 3 | ||
| rs963549 | 8 | 53229264 | synonymous variant | C/T | snv | 0.17 | 0.24 | 1 |