| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4468878 | 20 | 61353181 | intron variant | T/C | snv | 0.51 | 1 | ||||
| rs2024714 | 20 | 61637438 | intron variant | C/T | snv | 0.60 | 1 | ||||
| rs2427216 | 1.000 | 0.040 | 20 | 61639158 | intron variant | C/A;T | snv | 1 | |||
| rs6061910 | 20 | 61933124 | splice region variant | G/A | snv | 1 |