| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs3766379 | 0.851 | 0.320 | 1 | 160837925 | intron variant | T/C | snv | 0.57 | 4 | ||
| rs6682654 | 0.882 | 0.320 | 1 | 160839213 | intron variant | G/A | snv | 0.45 | 3 |