| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
| rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 13 | ||
| rs2280401 | 19 | 49496752 | intron variant | G/A | snv | 0.12 | 5 | ||||
| rs4561508 | 17 | 16945436 | intron variant | C/T | snv | 0.12 | 3 | ||||
| rs10097731 | 8 | 81115437 | upstream gene variant | G/T | snv | 0.12 | 1 | ||||
| rs3777200 | 5 | 95899087 | intron variant | C/T | snv | 0.31 | 1 |