| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137853883 | 0.882 | 0.120 | 17 | 41819307 | frameshift variant | C/-;CC | delins | 5 | |||
| rs397509383 | 0.925 | 0.120 | 17 | 41820961 | frameshift variant | CC/A | delins | 2 | |||
| rs1555616552 | 1.000 | 0.120 | 17 | 41819220 | frameshift variant | C/-;CC | delins | 1 | |||
| rs1567856056 | 1.000 | 0.120 | 17 | 41820960 | frameshift variant | -/C | delins | 1 | |||
| rs387906960 | 1.000 | 0.120 | 17 | 41817156 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs397514674 | 1.000 | 0.120 | 17 | 41817149 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs782653042 | 1.000 | 0.120 | 17 | 41818104 | missense variant | C/T | snv | 2.0E-05 | 5.6E-05 | 1 | |
| rs869320752 | 1.000 | 0.120 | 17 | 41819357 | inframe deletion | TAC/- | delins | 1 |