| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 9 | |||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
| rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 8 | ||
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 8 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 7 | ||
| 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 | ||||
| rs583104 | 1 | 109278685 | downstream gene variant | G/T | snv | 0.63 | 6 | ||||
| rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 5 | ||
| rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
| rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
| rs9436735 | 1 | 65419378 | upstream gene variant | C/G | snv | 2.5E-02 | 5 | ||||
| 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 | ||
| rs6668858 | 1 | 204166660 | intron variant | G/A | snv | 9.7E-03 | 4 | ||||
| rs12097137 | 1 | 101243889 | downstream gene variant | G/A;T | snv | 3 | |||||
| rs17315646 | 1 | 230159560 | intron variant | C/A;G | snv | 0.45 | 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 | |||||
| rs2308939 | 1 | 15506955 | missense variant | G/A;C;T | snv | 3.3E-04 | 3 | ||||
| rs235216 | 1 | 12209567 | downstream gene variant | C/A;G;T | snv | 3 | |||||
| rs2819325 | 1 | 162313721 | intron variant | G/A;C | snv | 3 |