Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
| rs1217407 | 1.000 | 0.120 | 1 | 113851126 | intron variant | A/G | snv | 0.77 | 1 | ||
| rs1217418 | 0.925 | 0.120 | 1 | 113858609 | intron variant | A/G | snv | 0.53 | 0.57 | 1 | |
| rs1217413 | 1.000 | 0.120 | 1 | 113815128 | intron variant | G/A | snv | 0.82 | 1 |