| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1565331646 | 1.000 | 0.120 | 11 | 72107947 | frameshift variant | -/CTCG | delins | 2 | |||
| rs137853188 | 1.000 | 0.120 | 11 | 72106185 | stop gained | C/G | snv | 1 | |||
| rs137853187 | 1.000 | 0.120 | 11 | 72106180 | missense variant | G/A | snv | 3.6E-05 | 3.5E-05 | 1 | |
| rs545947177 | 1.000 | 0.120 | 11 | 72106214 | splice region variant | A/C | snv | 4.5E-05 | 2.1E-05 | 1 | |
| rs137853185 | 1.000 | 0.120 | 11 | 72106094 | missense variant | G/A | snv | 2.6E-05 | 1.4E-05 | 1 | |
| rs137853186 | 1.000 | 0.120 | 11 | 72106165 | missense variant | T/C | snv | 1 |