Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2154393 | 1.000 | 0.040 | 10 | 60566929 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
| rs3808943 | 0.925 | 0.040 | 10 | 60391257 | intron variant | C/T | snv | 9.7E-02 | 1 | ||
| rs4948412 | 1.000 | 0.040 | 10 | 60386818 | intron variant | T/C | snv | 7.3E-02 | 1 | ||
| rs4948417 | 1.000 | 0.040 | 10 | 60401860 | intron variant | A/G | snv | 9.7E-02 | 1 | ||
| rs4948418 | 0.925 | 0.040 | 10 | 60425736 | intron variant | C/T | snv | 7.9E-02 | 1 | ||
| rs9633553 | 1.000 | 0.040 | 10 | 60514979 | intron variant | T/G | snv | 8.3E-02 | 1 |