Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 5 | ||
| rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 3 | |
| rs287 | 8 | 19958045 | intron variant | A/G;T | snv | 3 | |||||
| rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 3 | |
| rs1059611 | 8 | 19967052 | 3 prime UTR variant | T/C | snv | 0.13 | 2 | ||||
| rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 2 | ||||
| rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 2 | |||
| rs264 | 0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 | 2 | ||
| rs325 | 8 | 19961817 | intron variant | T/C | snv | 9.0E-02 | 2 | ||||
| rs326 | 8 | 19961928 | intron variant | A/G | snv | 0.37 | 2 | ||||
| rs7016529 | 8 | 19949120 | intron variant | T/C | snv | 8.4E-02 | 2 | ||||
| rs11570891 | 8 | 19965299 | intron variant | C/T | snv | 9.5E-02; 2.1E-04 | 9.4E-02 | 1 | |||
| rs263 | 1.000 | 0.040 | 8 | 19955301 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs271 | 1.000 | 0.040 | 8 | 19956191 | intron variant | G/A;T | snv | 1 | |||
| rs301 | 0.925 | 0.160 | 8 | 19959423 | intron variant | T/C | snv | 0.24 | 0.26 | 1 | |
| rs3289 | 8 | 19965681 | 3 prime UTR variant | T/C | snv | 4.0E-02 | 1 | ||||
| rs331 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 1 |