| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
| rs7759938 | 0.925 | 0.120 | 6 | 104931079 | intron variant | C/T | snv | 0.62 | 4 | ||
| rs314263 | 6 | 104944870 | intron variant | C/T | snv | 0.69 | 3 | ||||
| rs11217863 | 11 | 120422429 | intron variant | G/A | snv | 8.6E-02 | 2 | ||||
| rs154001 | 1.000 | 0.040 | 5 | 128349443 | missense variant | C/G;T | snv | 0.73 | 2 | ||
| rs34952318 | 20 | 11196407 | regulatory region variant | G/A | snv | 4.6E-02 | 2 | ||||
| rs722585 | 6 | 1775629 | intron variant | G/A | snv | 0.25 | 2 |