| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909800 | 0.807 | 0.360 | 12 | 47844859 | missense variant | G/A;T | snv | 6 | |||
| rs121909796 | 0.827 | 0.200 | 12 | 47846743 | missense variant | C/A | snv | 5 | |||
| rs121909798 | 0.925 | 0.200 | 12 | 47846444 | missense variant | G/C | snv | 2 | |||
| rs121909799 | 0.925 | 0.200 | 12 | 47846418 | missense variant | A/C | snv | 5.4E-06 | 2 | ||
| rs121909801 | 0.925 | 0.200 | 12 | 47879026 | stop gained | G/A;C | snv | 1.6E-05 | 2 | ||
| rs886037890 | 0.925 | 0.200 | 12 | 47844840 | missense variant | T/G | snv | 2 | |||
| rs121909790 | 1.000 | 0.200 | 12 | 47879016 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs121909791 | 1.000 | 0.200 | 12 | 47865106 | missense variant | C/T | snv | 3.6E-05 | 3.5E-05 | 1 | |
| rs121909792 | 1.000 | 0.200 | 12 | 47846679 | stop gained | G/T | snv | 4.0E-06 | 1 | ||
| rs121909793 | 1.000 | 0.200 | 12 | 47865085 | missense variant | C/T | snv | 1 | |||
| rs121909794 | 1.000 | 0.200 | 12 | 47865175 | missense variant | C/T | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs121909795 | 1.000 | 0.200 | 12 | 47857512 | stop gained | G/A | snv | 1 | |||
| rs121909797 | 1.000 | 0.200 | 12 | 47878977 | missense variant | C/A;G;T | snv | 2.4E-05; 4.0E-06 | 1 | ||
| rs121909802 | 1.000 | 0.200 | 12 | 47846374 | stop gained | C/A;T | snv | 1 | |||
| rs267607169 | 1.000 | 0.200 | 12 | 47844994 | missense variant | C/T | snv | 4.0E-06 | 1 |