| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61755783 | 0.763 | 0.080 | 6 | 42721911 | missense variant | G/A | snv | 1.4E-05 | 11 | ||
| rs61750641 | 0.790 | 0.080 | 1 | 94005499 | missense variant | C/T | snv | 3.5E-04 | 4.7E-04 | 7 | |
| rs764759172 | 0.925 | 0.040 | 1 | 94080692 | frameshift variant | G/- | del | 3 | |||
| rs1402837406 | 0.882 | 0.080 | 9 | 2718093 | frameshift variant | CC/-;CCC | delins | 2.8E-05 | 3 | ||
| rs1557106557 | 1.000 | 0.040 | X | 49212756 | missense variant | G/A | snv | 2 | |||
| rs1306231185 | 0.925 | 0.120 | 20 | 10407645 | stop gained | -/TTCA | delins | 4.0E-06 | 7.0E-06 | 2 |