Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17632578 | 1.000 | 0.040 | 6 | 117341781 | intron variant | C/T | snv | 9.5E-02 | 1 | ||
| rs1894674 | 1.000 | 0.040 | 6 | 117338690 | intron variant | C/G | snv | 9.7E-02 | 1 | ||
| rs2157535 | 1.000 | 0.040 | 6 | 117347826 | intron variant | G/A | snv | 0.79 | 1 | ||
| rs2301485 | 1.000 | 0.040 | 6 | 117340261 | intron variant | A/G | snv | 9.6E-02 | 1 | ||
| rs3798379 | 1.000 | 0.040 | 6 | 117346046 | intron variant | T/C | snv | 0.15 | 1 |