| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10975003 | 0.882 | 0.080 | 9 | 5213687 | intergenic variant | T/C | snv | 0.43 | 1 | ||
| rs11133504 | 1.000 | 0.040 | 4 | 57514156 | intergenic variant | G/A | snv | 0.23 | 1 | ||
| rs11739663 | 1.000 | 0.040 | 5 | 593968 | intergenic variant | T/C | snv | 0.29 | 1 | ||
| rs13361189 | 0.752 | 0.240 | 5 | 150843825 | upstream gene variant | T/C | snv | 0.21 | 1 | ||
| rs1456893 | 0.851 | 0.160 | 7 | 50230076 | intron variant | G/A | snv | 0.69 | 1 | ||
| rs1495965 | 0.790 | 0.280 | 1 | 67287825 | intergenic variant | C/T | snv | 0.55 | 1 | ||
| rs16940186 | 1.000 | 0.040 | 16 | 85976134 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs17234657 | 0.882 | 0.120 | 5 | 40401407 | intergenic variant | T/G | snv | 0.14 | 1 | ||
| rs17771967 | 1.000 | 0.040 | 19 | 54868759 | downstream gene variant | A/G | snv | 0.42 | 1 | ||
| rs1830610 | 1.000 | 0.040 | 9 | 5260079 | intergenic variant | C/G;T | snv | 1 | |||
| rs2108225 | 1.000 | 0.040 | 7 | 107812658 | downstream gene variant | G/A;T | snv | 1 | |||
| rs2457996 | 1.000 | 0.040 | 4 | 73990818 | upstream gene variant | C/A;G;T | snv | 1 | |||
| rs3129891 | 0.851 | 0.160 | 6 | 32447303 | downstream gene variant | G/A | snv | 0.20 | 1 | ||
| rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 1 | |||
| rs4510766 | 1.000 | 0.040 | 7 | 107852344 | intergenic variant | A/G | snv | 0.36 | 1 | ||
| rs4722672 | 1.000 | 0.040 | 7 | 27192143 | intron variant | C/T | snv | 0.73 | 1 | ||
| rs4957048 | 0.925 | 0.120 | 5 | 583327 | intergenic variant | G/A | snv | 0.16 | 1 | ||
| rs549182 | 0.925 | 0.160 | 6 | 32237268 | intergenic variant | G/A | snv | 4.5E-02 | 1 | ||
| rs6451493 | 1.000 | 0.040 | 5 | 40410833 | upstream gene variant | G/A;T | snv | 1 | |||
| rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 1 | ||
| rs7720838 | 0.925 | 0.040 | 5 | 40486794 | intron variant | G/T | snv | 0.52 | 1 | ||
| rs7869487 | 0.882 | 0.040 | 9 | 114818634 | intergenic variant | C/G;T | snv | 1 | |||
| rs7911117 | 1.000 | 0.040 | 10 | 26890667 | regulatory region variant | T/G | snv | 0.18 | 1 | ||
| rs886774 | 1.000 | 0.040 | 7 | 107854989 | regulatory region variant | G/A | snv | 0.67 | 1 | ||
| rs9271209 | 1.000 | 0.040 | 6 | 32611258 | intergenic variant | G/A | snv | 0.74 | 1 |