| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
| rs974173968 | 0.882 | 0.080 | 10 | 121551382 | missense variant | G/A;T | snv | 8.0E-06 | 3 | ||
| rs746082633 | 0.827 | 0.280 | 8 | 38418270 | missense variant | T/C | snv | 1.6E-05 | 1.4E-05 | 5 | |
| rs780497781 | 0.925 | 0.080 | 10 | 121479954 | missense variant | C/T | snv | 2.4E-05 | 2.8E-05 | 2 |