| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 17 | |||
| rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 11 | |||
| rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 6 | |||
| rs2200733 | 0.752 | 0.240 | 4 | 110789013 | intergenic variant | C/T | snv | 0.18 | 4 | ||
| rs13143308 | 0.882 | 0.120 | 4 | 110793263 | upstream gene variant | T/C;G | snv | 3 | |||
| rs12932445 | 0.925 | 0.080 | 16 | 73035989 | intron variant | T/C | snv | 0.18 | 2 | ||
| rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 1 | ||
| rs16939239 | 1.000 | 8 | 76122993 | intergenic variant | G/A | snv | 0.14 | 1 | |||
| rs638704 | 1.000 | 1 | 170629046 | intron variant | C/T | snv | 0.64 | 1 | |||
| rs6891174 | 0.925 | 0.040 | 5 | 173213587 | intergenic variant | A/G | snv | 0.73 | 1 | ||
| rs4727833 | 1.000 | 7 | 116507854 | 3 prime UTR variant | C/G;T | snv | 1 | ||||
| rs11596587 | 1.000 | 10 | 69354232 | intron variant | C/T | snv | 0.11 | 1 | |||
| rs74154533 | 1.000 | 10 | 103547967 | intron variant | G/A | snv | 0.17 | 1 | |||
| rs146390073 | 1.000 | 1 | 241142948 | intron variant | C/T | snv | 1.1E-02 | 1 |