| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5030820 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
| rs5030824 | 0.776 | 0.320 | 3 | 10149885 | missense variant | C/G | snv | 2.0E-05 | 4.2E-05 | 5 | |
| rs104893826 | 0.882 | 0.200 | 3 | 10142038 | missense variant | G/A;C | snv | 4 | |||
| rs397516440 | 0.851 | 0.280 | 3 | 10142166 | missense variant | C/G;T | snv | 4.5E-06 | 4 | ||
| rs5030823 | 0.851 | 0.280 | 3 | 10149871 | stop gained | C/A;G;T | snv | 4.0E-06 | 4 | ||
| rs5030808 | 0.882 | 0.200 | 3 | 10142124 | missense variant | G/A;C;T | snv | 4.5E-06 | 3 | ||
| rs864321642 | 0.925 | 0.160 | 3 | 10149832 | missense variant | T/A;C | snv | 2 | |||
| rs864321643 | 0.925 | 0.160 | 3 | 10142140 | missense variant | A/C;G | snv | 2 |