| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
| rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
| rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 4 | ||||
| rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 4 | ||
| rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 4 | ||
| rs7518199 | 1 | 154434943 | intron variant | A/C;T | snv | 0.39; 4.2E-06 | 4 | ||||
| rs7529229 | 0.851 | 0.120 | 1 | 154448302 | intron variant | T/C | snv | 0.48 | 4 |