Source: CLINVAR
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1553265736 | 0.925 | 0.040 | 1 | 156136080 | missense variant | G/C | snv | 4 | |||
| rs56793579 | 0.851 | 0.240 | 1 | 156115102 | missense variant | C/G;T | snv | 3 | |||
| rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 3 | |||
| rs794728602 | 1.000 | 0.040 | 1 | 156115168 | missense variant | G/A | snv | 3 |