| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137853202 | 1.000 | 0.040 | 2 | 85663814 | missense variant | G/A | snv | 2.9E-05 | 1.5E-04 | 1 | |
| rs1553380888 | 1.000 | 0.040 | 2 | 85665723 | synonymous variant | C/A | snv | 1 | |||
| rs1558572491 | 1.000 | 0.040 | 2 | 85661536 | splice acceptor variant | C/T | snv | 1 | |||
| rs35328240 | 1.000 | 0.040 | 2 | 85666649 | frameshift variant | G/TTC | delins | 1 | |||
| rs779795223 | 1.000 | 0.040 | 2 | 85666648 | frameshift variant | -/TT | ins | 2.2E-04 | 2.4E-04 | 1 |