| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 8 | ||
| rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
| rs4970834 | 0.925 | 0.160 | 1 | 109272258 | intron variant | C/T | snv | 0.17 | 0.21 | 6 | |
| rs5176 | 1 | 53246137 | 3 prime UTR variant | T/G | snv | 6.4E-04 | 6 | ||||
| rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 | |||||
| rs11207997 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 5 | ||||
| rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 5 | ||||
| rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 5 | ||
| rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
| rs1748197 | 1 | 62590441 | intron variant | G/A | snv | 0.42 | 5 | ||||
| rs2131925 | 1 | 62560271 | intron variant | G/T | snv | 0.57 | 5 | ||||
| rs11465759 | 1 | 67166721 | intron variant | T/G | snv | 2.4E-02 | 4 | ||||
| rs11571111 | 1 | 204161105 | intron variant | C/A | snv | 5.0E-03 | 4 | ||||
| rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 4 | ||
| rs4846914 | 0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 | 4 | ||
| rs567279 | 1 | 66222346 | intron variant | G/T | snv | 0.97 | 4 | ||||
| rs585362 | 1 | 109247173 | upstream gene variant | C/G;T | snv | 4 | |||||
| rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 4 | |
| rs6668858 | 1 | 204166660 | intron variant | G/A | snv | 9.7E-03 | 4 | ||||
| rs734359 | 1 | 41480231 | intron variant | C/T | snv | 7.5E-02 | 4 | ||||
| rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 3 | |||||
| rs17315646 | 1 | 230159560 | intron variant | C/A;G | snv | 0.45 | 3 | ||||
| rs1748195 | 0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv | 3 | |||
| rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 3 | ||
| rs2296065 | 1 | 230166030 | intron variant | G/A;C | snv | 3 |