| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 22 | |
| rs75603564 | 14 | 89038109 | intergenic variant | C/T | snv | 3.4E-02 | 2 | ||||
| rs2673604 | 8 | 132399360 | intron variant | C/A | snv | 0.62 | 1 | ||||
| rs11634944 | 15 | 24937946 | intron variant | T/C | snv | 0.34 | 1 | ||||
| rs74439372 | 11 | 5615470 | intron variant | AC/- | delins | 0.80 | 1 |