Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3757318 | 0.882 | 0.160 | 6 | 151592978 | intron variant | G/A | snv | 6.1E-02 | 1 | ||
| rs3757322 | 1.000 | 0.080 | 6 | 151621059 | 3 prime UTR variant | T/G | snv | 0.36 | 1 | ||
| rs1038304 | 0.882 | 0.160 | 6 | 151612040 | intron variant | A/G | snv | 0.58 | 1 | ||
| rs3734805 | 0.925 | 0.080 | 6 | 151618215 | 3 prime UTR variant | A/C | snv | 6.9E-02 | 1 | ||
| rs6929137 | 0.851 | 0.160 | 6 | 151615542 | missense variant | G/A | snv | 0.31 | 0.36 | 1 |