| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907196 | 0.807 | 0.080 | 9 | 37784953 | missense variant | C/G | snv | 2.0E-05 | 12 | ||
| rs141138948 | 0.807 | 0.120 | 9 | 37783993 | missense variant | T/C;G | snv | 4.1E-04 | 9 | ||
| rs374550999 | 0.925 | 0.080 | 9 | 37784807 | missense variant | C/A;G | snv | 1.5E-04 | 2 | ||
| rs387907195 | 1.000 | 9 | 37783973 | missense variant | C/G | snv | 8.0E-06 | 1 | |||
| rs587780333 | 1.000 | 9 | 37784933 | frameshift variant | C/- | delins | 4.1E-06 | 1.4E-05 | 1 | ||
| rs672601331 | 1.000 | 9 | 37784742 | frameshift variant | AGTAAACACC/- | delins | 1 | ||||
| rs730882145 | 1.000 | 9 | 37782041 | missense variant | C/A;T | snv | 1.2E-05 | 1 | |||
| rs797045567 | 1.000 | 9 | 37782040 | missense variant | C/T | snv | 8.0E-06 | 1 | |||
| rs886041316 | 1.000 | 9 | 37784890 | frameshift variant | G/- | delins | 8.6E-06 | 1.4E-05 | 1 | ||
| rs672601332 | 1.000 | 9 | 37780795 | missense variant | A/G | snv | 1 | ||||
| rs1566696845 | 1.000 | 14 | 96833625 | splice donor variant | TCTTGGTA/- | delins | 1 |