| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1398830127 | 0.925 | 0.080 | 6 | 29610981 | missense variant | C/T | snv | 4.1E-06 | 2 | ||
| rs1805057 | 0.925 | 0.080 | 6 | 29613344 | missense variant | C/T | snv | 1.1E-03 | 1.5E-03 | 2 | |
| rs2020918 | 0.925 | 0.080 | 8 | 42214920 | intergenic variant | A/G | snv | 0.71 | 2 | ||
| rs137852779 | 1.000 | 0.040 | 6 | 52438538 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs11191692 | 1.000 | 0.040 | 10 | 103454008 | 3 prime UTR variant | G/A | snv | 0.29 | 1 | ||
| rs2302515 | 1.000 | 0.040 | 12 | 7652640 | missense variant | C/G | snv | 0.78 | 0.76 | 1 | |
| rs844347 | 1.000 | 0.040 | 12 | 50067893 | intron variant | A/C | snv | 0.32 | 1 | ||
| rs944688 | 1.000 | 0.040 | 9 | 98601678 | intron variant | C/T | snv | 0.35 | 1 |