| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs542652468 | 0.882 | 19 | 41986177 | missense variant | G/A;T | snv | 6 | ||||
| rs1569234334 | 0.851 | 0.200 | X | 70329420 | missense variant | G/T | snv | 5 | |||
| rs1085308053 | 0.882 | 0.080 | 10 | 87952230 | missense variant | C/T | snv | 5 | |||
| rs564185858 | 0.882 | 0.040 | 10 | 110122249 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 4 | |
| rs121912708 | 1.000 | 0.040 | 5 | 126583997 | stop gained | G/A;C | snv | 6.0E-05; 4.0E-06 | 3 | ||
| rs140845195 | 1.000 | 0.040 | 5 | 126545020 | splice acceptor variant | C/A;T | snv | 1.6E-05; 4.0E-06 | 3 | ||
| rs1559720382 | 1.000 | 3 | 47101476 | missense variant | T/C | snv | 2 |