Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7977418 | 12 | 28435309 | intron variant | T/C | snv | 0.40 | 3 | ||||
| rs2348418 | 12 | 28536581 | intron variant | T/C | snv | 0.40 | 2 | ||||
| rs200840970 | 12 | 28444850 | intron variant | TT/-;T;TTT | delins | 2.4E-03 | 1 | ||||
| rs191000678 | 12 | 28134057 | intron variant | A/T | snv | 1.6E-03 | 1 |