Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs132570 | 1.000 | 0.040 | 22 | 39580123 | intron variant | C/A | snv | 0.45 | 2 | ||
| rs5757730 | 1.000 | 0.040 | 22 | 39571425 | intron variant | A/G | snv | 0.55 | 2 | ||
| rs132575 | 1.000 | 0.040 | 22 | 39586716 | intron variant | A/G | snv | 0.51 | 1 | ||
| rs3788556 | 22 | 39576157 | intron variant | T/C | snv | 0.60 | 1 | ||||
| rs3788568 | 22 | 39615268 | intron variant | G/A;T | snv | 1 | |||||
| rs5750853 | 22 | 39580181 | intron variant | C/T | snv | 0.36 | 1 | ||||
| rs5750854 | 22 | 39594770 | intron variant | C/T | snv | 0.22 | 1 |