Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 7 | |
| rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 5 | ||||
| rs301 | 0.925 | 0.160 | 8 | 19959423 | intron variant | T/C | snv | 0.24 | 0.26 | 5 | |
| 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 | |
| rs325 | 8 | 19961817 | intron variant | T/C | snv | 9.0E-02 | 4 | ||||
| rs327 | 8 | 19962025 | intron variant | T/G | snv | 0.31 | 4 | ||||
| rs3735964 | 1.000 | 0.080 | 8 | 19966534 | 3 prime UTR variant | C/A | snv | 9.1E-02 | 4 | ||
| rs1031045 | 8 | 19943601 | intron variant | G/A | snv | 0.12 | 3 | ||||
| rs1059507 | 1.000 | 0.080 | 8 | 19966452 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
| rs11570892 | 8 | 19966106 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
| rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 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 | ||||
| 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 | ||
| rs271 | 1.000 | 0.040 | 8 | 19956191 | intron variant | G/A;T | snv | 3 | |||
| rs28445964 | 8 | 19947085 | intron variant | A/G | snv | 7.0E-02 | 3 | ||||
| rs285 | 1.000 | 0.080 | 8 | 19957678 | intron variant | C/T | snv | 0.59 | 3 | ||
| rs28575919 | 8 | 19945458 | intron variant | C/G | snv | 7.7E-02 | 3 | ||||
| rs28615996 | 8 | 19945200 | intron variant | T/C | snv | 9.1E-02 | 3 |