| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28933368 | 0.851 | 0.080 | 17 | 39725721 | missense variant | G/A | snv | 1 | |||
| rs1057519903 | 0.683 | 0.080 | 1 | 226064434 | missense variant | A/T | snv | 1 | |||
| rs1553260624 | 0.763 | 0.080 | 1 | 226064454 | missense variant | G/A | snv | 1 | |||
| rs1057519904 | 0.742 | 0.080 | 6 | 27872233 | missense variant | T/A | snv | 1 | |||
| rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 1 | |||
| rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 1 | |||
| rs776893978 | 22 | 20997253 | missense variant | C/T | snv | 4.4E-05 | 9.1E-05 | 1 | |||
| rs869320686 | 0.882 | 22 | 20990476 | missense variant | G/A | snv | 1 | ||||
| rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 1 | ||
| rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs28934578 | 0.605 | 0.600 | 17 | 7675088 | missense variant | C/A;T | snv | 4.0E-06 | 1 |