| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11749391 | 0.827 | 0.120 | 5 | 150849504 | intron variant | T/C | snv | 0.21 | 5 | ||
| rs11741861 | 0.925 | 0.040 | 5 | 150898347 | intron variant | A/G | snv | 8.8E-02 | 3 | ||
| rs7714584 | 1.000 | 0.040 | 5 | 150890858 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs1000113 | 0.925 | 0.040 | 5 | 150860514 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 1 |