Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs258 | 8 | 19954741 | intron variant | G/A;C;T | snv | 3 | |||||
| rs271 | 1.000 | 0.040 | 8 | 19956191 | intron variant | G/A;T | snv | 3 | |||
| rs28645722 | 8 | 19945383 | intron variant | G/A;T | snv | 3 | |||||
| rs4921683 | 8 | 19967557 | downstream gene variant | T/A | snv | 0.14 | 3 | ||||
| rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 3 | |||
| rs320 | 0.827 | 0.200 | 8 | 19961566 | intron variant | T/A;G | snv | 3 | |||
| rs9644636 | 8 | 19967385 | downstream gene variant | T/A;G | snv | 3 | |||||
| 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 | |
| rs325 | 8 | 19961817 | intron variant | T/C | snv | 9.0E-02 | 4 | ||||
| rs1470186 | 8 | 19938278 | intron variant | T/C | snv | 6.6E-02 | 3 | ||||
| rs255 | 8 | 19954390 | intron variant | T/C | snv | 0.17 | 0.18 | 3 | |||
| rs28615996 | 8 | 19945200 | intron variant | T/C | snv | 9.1E-02 | 3 | ||||
| rs3289 | 8 | 19965681 | 3 prime UTR variant | T/C | snv | 4.0E-02 | 3 | ||||
| rs6999612 | 8 | 19945573 | intron variant | T/C | snv | 7.8E-02 | 3 | ||||
| rs7009128 | 8 | 19930017 | intron variant | T/C | snv | 0.10 | 3 | ||||
| rs7016529 | 8 | 19949120 | intron variant | T/C | snv | 8.4E-02 | 3 | ||||
| rs327 | 8 | 19962025 | intron variant | T/G | snv | 0.31 | 4 | ||||
| rs1800590 | 8 | 19939160 | intron variant | T/G | snv | 0.13 | 3 | ||||
| rs10099160 | 8 | 19964304 | intron variant | T/G | snv | 0.20 | 2 |