| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
| rs1330 | 1.000 | 0.080 | 11 | 17294482 | intron variant | C/T | snv | 0.30 | 4 | ||
| rs806794 | 6 | 26200449 | 3 prime UTR variant | A/G | snv | 0.36 | 6 | ||||
| rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
| rs710841 | 4 | 81228677 | intergenic variant | C/T | snv | 0.37 | 3 | ||||
| rs224333 | 20 | 35436182 | intron variant | A/G | snv | 0.47 | 3 | ||||
| rs4896582 | 6 | 142382740 | intron variant | G/A | snv | 0.50 | 5 | ||||
| rs3738814 | 1 | 17005181 | intron variant | A/G | snv | 0.52 | 3 | ||||
| rs8007661 | 14 | 91993614 | intron variant | C/T | snv | 0.52 | 3 | ||||
| rs7141420 | 1.000 | 0.080 | 14 | 79433111 | intron variant | C/T | snv | 0.56 | 5 | ||
| rs7759938 | 0.925 | 0.120 | 6 | 104931079 | intron variant | C/T | snv | 0.62 | 7 | ||
| rs1759645 | 6 | 34227089 | TF binding site variant | C/T | snv | 0.71 | 3 | ||||
| rs395962 | 6 | 104949543 | intron variant | T/G | snv | 0.72 | 6 | ||||
| rs552707 | 7 | 28165684 | intron variant | T/C | snv | 0.77 | 2 | ||||
| rs1708299 | 7 | 28150327 | intron variant | A/G | snv | 0.77 | 3 | ||||
| rs606452 | 1.000 | 0.040 | 11 | 75565133 | intron variant | A/C | snv | 0.78 | 4 | ||
| rs7689420 | 0.851 | 0.080 | 4 | 144647200 | non coding transcript exon variant | T/C | snv | 0.79 | 7 | ||
| rs1812175 | 4 | 144653692 | intron variant | A/G | snv | 0.79 | 6 | ||||
| rs2780226 | 6 | 34231315 | regulatory region variant | C/T | snv | 0.80 | 3 |