| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs37369 | 0.807 | 0.120 | 5 | 35037010 | missense variant | C/T | snv | 0.21 | 0.25 | 1 | |
| rs398122917 | 0.882 | 0.080 | X | 155280059 | missense variant | G/C | snv | 4.4E-05 | 1.1E-04 | 1 | |
| rs587782951 | 0.807 | 0.080 | 20 | 44160305 | missense variant | G/T | snv | 1 | |||
| rs991104525 | 0.882 | 0.160 | 5 | 78969051 | missense variant | G/A | snv | 1.2E-05 | 7.7E-05 | 1 | |
| rs1559279177 | 0.851 | 0.160 | 1 | 146018661 | frameshift variant | G/- | del | 5 | |||
| rs748379243 | 0.882 | 0.200 | 5 | 60928961 | splice acceptor variant | T/A;C | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs587782927 | 0.882 | 0.080 | 6 | 7574084 | splice region variant | AG/- | delins | 4 | |||
| rs1799998 | 0.742 | 0.200 | 8 | 142918184 | upstream gene variant | A/G;T | snv | 0.38 | 1 |