| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1458103 | 11 | 81336231 | intron variant | A/C | snv | 0.25 | 1 | ||||
| rs16916239 | 8 | 86631513 | intron variant | A/G | snv | 0.16 | 1 | ||||
| rs1799964 | 0.608 | 0.760 | 6 | 31574531 | upstream gene variant | T/C | snv | 0.19 | 1 | ||
| rs2451828 | 5 | 7448683 | intron variant | C/T | snv | 2.7E-02 | 1 | ||||
| rs324981 | 0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 | 1 | |
| rs342422 | 5 | 84175168 | intron variant | G/A;C | snv | 1 | |||||
| rs34516333 | 16 | 73114768 | intron variant | G/T | snv | 0.17 | 1 | ||||
| rs356200 | 0.882 | 0.160 | 4 | 89747463 | intron variant | T/C | snv | 0.44 | 1 | ||
| rs356219 | 0.776 | 0.240 | 4 | 89716450 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs3918242 | 0.602 | 0.680 | 20 | 46007337 | upstream gene variant | C/T | snv | 0.14 | 1 | ||
| rs4692589 | 4 | 170014094 | intron variant | A/G | snv | 0.44 | 1 | ||||
| rs4951043 | 1 | 204105737 | intron variant | C/T | snv | 0.51 | 1 | ||||
| rs6030245 | 20 | 42441919 | intron variant | T/C | snv | 0.30 | 1 | ||||
| rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 1 | |||
| rs6462203 | 7 | 3636370 | intron variant | C/A;T | snv | 1 | |||||
| rs72711240 | 4 | 134774652 | intron variant | C/T | snv | 2.2E-02 | 1 | ||||
| rs79928194 | 2 | 232784580 | intron variant | T/C | snv | 0.14 | 1 | ||||
| rs9875578 | 3 | 13752941 | intergenic variant | G/A;C | snv | 1 |