| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1210124629 | 0.882 | 0.120 | 3 | 9944503 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs367652299 | 0.882 | 0.120 | 18 | 79411375 | missense variant | C/T | snv | 3.3E-05 | 2.1E-05 | 3 | |
| rs62096875 | 0.882 | 0.120 | 18 | 79410903 | missense variant | G/A;T | snv | 7.4E-04; 4.1E-06 | 3 | ||
| rs749275495 | 0.882 | 0.120 | 22 | 19764273 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 3 | |
| rs147232392 | 0.882 | 0.240 | X | 137566740 | missense variant | G/A;T | snv | 2.6E-03 | 3 | ||
| rs1274480565 | 0.925 | 0.120 | 22 | 19761154 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs201398331 | 0.925 | 0.120 | X | 137566789 | missense variant | C/T | snv | 1.1E-04 | 3.7E-05 | 2 | |
| rs563944253 | 1.000 | 0.120 | 13 | 20598654 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs542259595 | 1.000 | 0.120 | 18 | 79467576 | missense variant | G/A;T | snv | 1.6E-05; 2.0E-05 | 1 |