| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909210 | 0.708 | 0.200 | 5 | 136046406 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
| rs121909211 | 0.724 | 0.200 | 5 | 136046407 | missense variant | G/A;T | snv | 4.0E-05 | 15 | ||
| rs121909208 | 0.724 | 0.240 | 5 | 136056780 | missense variant | C/T | snv | 7.0E-06 | 13 | ||
| rs121909209 | 0.763 | 0.160 | 5 | 136056781 | missense variant | G/A | snv | 9 | |||
| rs121909215 | 0.790 | 0.200 | 5 | 136060898 | missense variant | G/A | snv | 7 | |||
| rs762267106 | 1.000 | 0.080 | 9 | 121328963 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 1 |