| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34410987 | 0.882 | 0.040 | 12 | 40283897 | missense variant | C/T | snv | 7.4E-04 | 2.2E-04 | 3 | |
| rs3738136 | 0.882 | 0.040 | 1 | 20645618 | missense variant | G/A | snv | 9.2E-02 | 5.0E-02 | 3 | |
| rs3758549 | 0.882 | 0.040 | 10 | 102244438 | upstream gene variant | G/A | snv | 0.14 | 3 | ||
| rs397515634 | 0.925 | 0.040 | 4 | 41256996 | missense variant | A/C | snv | 4.0E-06 | 3 | ||
| rs415430 | 1.000 | 0.040 | 17 | 46781778 | intron variant | C/T | snv | 0.84 | 3 | ||
| rs557074 | 1.000 | 0.040 | 6 | 7144958 | intron variant | T/G | snv | 0.27 | 3 | ||
| rs7215239 | 1.000 | 0.040 | 17 | 45690407 | intron variant | T/C | snv | 0.30 | 3 | ||
| rs72554080 | 0.925 | 0.040 | 2 | 232747740 | missense variant | A/G | snv | 2.6E-04 | 3.2E-04 | 3 | |
| rs74315356 | 0.925 | 0.040 | 1 | 20649054 | stop gained | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs74315359 | 0.882 | 0.040 | 1 | 20644651 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 3 | |
| rs816411 | 1.000 | 0.040 | 7 | 56103796 | intron variant | C/T | snv | 0.53 | 3 | ||
| rs823114 | 1.000 | 0.040 | 1 | 205750404 | upstream gene variant | G/A | snv | 0.45 | 3 | ||
| rs876658902 | 0.925 | 0.040 | 17 | 7676182 | missense variant | C/T | snv | 3 | |||
| rs947211 | 0.925 | 0.040 | 1 | 205783537 | non coding transcript exon variant | A/G | snv | 0.64 | 3 | ||
| rs10247962 | 1.000 | 0.040 | 7 | 100622306 | intron variant | G/A | snv | 0.88 | 2 | ||
| rs10445338 | 1.000 | 0.040 | 17 | 45990316 | intron variant | G/A | snv | 0.15 | 2 | ||
| rs10445364 | 1.000 | 0.040 | 17 | 45838990 | intron variant | G/A;C | snv | 2 | |||
| rs1057519492 | 0.925 | 0.040 | 17 | 5583798 | missense variant | C/T | snv | 2 | |||
| rs10746953 | 0.925 | 0.040 | 9 | 74302924 | regulatory region variant | C/T | snv | 0.44 | 2 | ||
| rs10788972 | 0.925 | 0.040 | 1 | 54106570 | intron variant | C/A | snv | 0.57 | 2 | ||
| rs10812774 | 0.925 | 0.040 | 9 | 28294233 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs11012 | 1.000 | 0.040 | 17 | 45436075 | 3 prime UTR variant | C/T | snv | 0.13 | 0.13 | 2 | |
| rs11107 | 1.000 | 0.040 | 22 | 32479203 | start lost | G/A;C | snv | 0.45; 8.0E-06 | 2 | ||
| rs111290936 | 0.925 | 0.040 | 3 | 184322089 | missense variant | C/T | snv | 7.2E-05 | 7.0E-05 | 2 | |
| rs111341148 | 0.925 | 0.040 | 12 | 40298346 | missense variant | G/A | snv | 3.2E-05 | 2.1E-05 | 2 |