| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1991866 | 8 | 129611859 | intron variant | G/A;C | snv | 1 | |||||
| rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 1 | ||
| rs2292982 | 1.000 | 0.120 | 16 | 85911217 | intron variant | T/C;G | snv | 1 | |||
| rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 1 |