| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs796065343 | 0.776 | 0.080 | 1 | 36467833 | missense variant | G/A | snv | 2 | |||
| rs606231473 | 1.000 | 1 | 36472313 | missense variant | G/A | snv | 2 | ||||
| rs1057519776 | 1.000 | 0.080 | 1 | 36467843 | missense variant | T/C | snv | 1 | |||
| rs121918426 | 0.882 | 0.080 | 1 | 36467597 | missense variant | G/A;T | snv | 4.1E-04 | 1 | ||
| rs890101650 | 1.000 | 1 | 36471501 | frameshift variant | -/C | delins | 4.0E-06 | 1 | |||
| rs879253750 | 1.000 | 1 | 36472141 | splice acceptor variant | T/A | snv | 1 | ||||
| rs606231474 | 1.000 | 1 | 36471473 | frameshift variant | C/- | delins | 1 | ||||
| rs759302795 | 1.000 | 1 | 36472561 | frameshift variant | C/- | del | 7.0E-06 | 1 | |||
| rs138156467 | 1.000 | 1 | 36468158 | stop gained | C/T | snv | 2.6E-04 | 2.6E-04 | 1 | ||
| rs606231475 | 1.000 | 1 | 36472272 | frameshift variant | TCGCTCCAGTGGCCAG/- | delins | 1 |