Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 5 | ||
| rs10994397 | 0.851 | 0.040 | 10 | 60519366 | intron variant | C/T | snv | 9.5E-02 | 5 | ||
| rs10994318 | 0.925 | 0.040 | 10 | 60366098 | intron variant | G/C | snv | 7.3E-02 | 2 | ||
| rs10994338 | 0.882 | 0.040 | 10 | 60421370 | intron variant | G/A | snv | 7.5E-02 | 2 | ||
| rs10994299 | 1.000 | 0.040 | 10 | 60316870 | intron variant | C/A | snv | 6.8E-02 | 1 | ||
| rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
| rs10994415 | 1.000 | 0.040 | 10 | 60562276 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs1938526 | 0.882 | 0.040 | 10 | 60540625 | intron variant | A/G | snv | 8.3E-02 | 1 | ||
| rs4948418 | 0.925 | 0.040 | 10 | 60425736 | intron variant | C/T | snv | 7.9E-02 | 1 |