| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777732 | 0.763 | 0.240 | 20 | 44406195 | missense variant | C/T | snv | 9 | |||
| rs776489992 | 1.000 | 0.040 | 20 | 44424133 | inframe deletion | TGC/-;TGCTGC | delins | 1.4E-04 | 1 | ||
| rs1555813319 | 1.000 | 0.040 | 20 | 44406208 | missense variant | G/A | snv | 1 |