| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34101942 | 1.000 | 0.160 | 22 | 39167907 | intergenic variant | -/A | delins | 0.68 | 1 | ||
| rs577040336 | 1.000 | 0.160 | 3 | 41856512 | intron variant | -/AATATATATATA | delins | 1 | |||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs201957963 | 1.000 | 0.160 | 3 | 41765956 | intron variant | -/TA | delins | 1 | |||
| rs587780174 | 0.827 | 0.360 | 22 | 28695239 | frameshift variant | A/- | delins | 4.4E-05 | 5.6E-05 | 7 | |
| rs6457327 | 0.790 | 0.320 | 6 | 31106253 | downstream gene variant | A/C | snv | 0.66 | 7 | ||
| rs4459895 | 0.827 | 0.160 | 3 | 188236626 | intron variant | A/C | snv | 0.88 | 5 | ||
| rs4240807 | 0.851 | 0.160 | 16 | 85951755 | downstream gene variant | A/C | snv | 0.76 | 4 | ||
| rs11129935 | 1.000 | 0.160 | 3 | 41943711 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs1128226 | 1.000 | 0.160 | 7 | 21902051 | 3 prime UTR variant | A/C | snv | 0.34 | 1 | ||
| rs113683976 | 1.000 | 0.160 | 3 | 41809193 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs11709840 | 1.000 | 0.160 | 3 | 169852453 | intron variant | A/C | snv | 0.28 | 1 | ||
| rs12185934 | 1.000 | 0.160 | 3 | 41795066 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs12330747 | 1.000 | 0.160 | 3 | 41949337 | intron variant | A/C | snv | 0.64 | 1 | ||
| rs1716642 | 1.000 | 0.160 | 3 | 41924373 | intron variant | A/C | snv | 0.68 | 1 | ||
| rs1717017 | 1.000 | 0.160 | 3 | 41874124 | intron variant | A/C | snv | 0.32 | 1 | ||
| rs17215988 | 1.000 | 0.160 | 3 | 41809828 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs17217536 | 1.000 | 0.160 | 3 | 41881808 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs4299460 | 1.000 | 0.160 | 3 | 41910953 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs4547673 | 1.000 | 0.160 | 3 | 41910811 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs55744136 | 1.000 | 0.160 | 3 | 41770801 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs56201224 | 1.000 | 0.160 | 3 | 41962935 | upstream gene variant | A/C | snv | 0.14 | 1 | ||
| rs57525756 | 1.000 | 0.160 | 3 | 41802099 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs6809328 | 1.000 | 0.160 | 3 | 41709513 | intron variant | A/C | snv | 0.21 | 1 | ||
| rs73071203 | 1.000 | 0.160 | 3 | 41935972 | intron variant | A/C | snv | 0.13 | 0.15 | 1 |