| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11031006 | 0.882 | 0.120 | 11 | 30204981 | intron variant | G/A | snv | 0.11 | 7 | ||
| rs16991615 | 0.925 | 0.080 | 20 | 5967581 | missense variant | G/A | snv | 4.5E-02 | 4.2E-02 | 6 | |
| rs72709458 | 0.882 | 0.040 | 5 | 1283640 | intron variant | C/A;T | snv | 5 |