Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7009128 | 8 | 19930017 | intron variant | T/C | snv | 0.10 | 3 | ||||
| rs1470186 | 8 | 19938278 | intron variant | T/C | snv | 6.6E-02 | 3 | ||||
| rs17091742 | 8 | 19938619 | intron variant | C/T | snv | 6.8E-02 | 3 | ||||
| rs1800590 | 8 | 19939160 | intron variant | T/G | snv | 0.13 | 3 | ||||
| rs1031045 | 8 | 19943601 | intron variant | G/A | snv | 0.12 | 3 | ||||
| rs28615996 | 8 | 19945200 | intron variant | T/C | snv | 9.1E-02 | 3 | ||||
| rs28645722 | 8 | 19945383 | intron variant | G/A;T | snv | 3 | |||||
| rs28575919 | 8 | 19945458 | intron variant | C/G | snv | 7.7E-02 | 3 | ||||
| rs6999612 | 8 | 19945573 | intron variant | T/C | snv | 7.8E-02 | 3 | ||||
| rs3779788 | 8 | 19945582 | intron variant | C/T | snv | 0.11 | 3 | ||||
| rs7000460 | 8 | 19946291 | intron variant | A/C | snv | 7.9E-02 | 3 | ||||
| rs28445964 | 8 | 19947085 | intron variant | A/G | snv | 7.0E-02 | 3 | ||||
| rs7016529 | 8 | 19949120 | intron variant | T/C | snv | 8.4E-02 | 3 | ||||
| rs343 | 1.000 | 0.080 | 8 | 19953276 | intron variant | C/A | snv | 9.8E-02 | 8.1E-02 | 3 | |
| rs253 | 1.000 | 0.040 | 8 | 19953906 | intron variant | C/T | snv | 0.53 | 3 | ||
| rs255 | 8 | 19954390 | intron variant | T/C | snv | 0.17 | 0.18 | 3 | |||
| rs256 | 8 | 19954456 | intron variant | C/T | snv | 0.12 | 3 | ||||
| rs258 | 8 | 19954741 | intron variant | G/A;C;T | snv | 3 | |||||
| rs263 | 1.000 | 0.040 | 8 | 19955301 | intron variant | C/T | snv | 0.23 | 3 | ||
| rs264 | 0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 | 4 | ||
| rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 4 | |
| rs271 | 1.000 | 0.040 | 8 | 19956191 | intron variant | G/A;T | snv | 3 | |||
| rs285 | 1.000 | 0.080 | 8 | 19957678 | intron variant | C/T | snv | 0.59 | 3 | ||
| rs301 | 0.925 | 0.160 | 8 | 19959423 | intron variant | T/C | snv | 0.24 | 0.26 | 5 | |
| rs316 | 8 | 19960925 | missense variant | C/A;T | snv | 0.13; 4.0E-06 | 3 |