| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4961 | 0.683 | 0.400 | 4 | 2904980 | missense variant | G/A;T | snv | 1.2E-05; 0.20 | 27 | ||
| rs1334067073 | 0.925 | 0.120 | 17 | 63478025 | missense variant | C/G;T | snv | 4.2E-06 | 2 | ||
| rs553553817 | 1.000 | 0.120 | 4 | 2882046 | missense variant | C/T | snv | 8.3E-06 | 1 |