Source: CLINVAR
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907351 | 1.000 | 7 | 2944495 | missense variant | T/C | snv | 7.0E-06 | 1 | |||
| rs571517554 | 1.000 | 7 | 2944528 | missense variant | C/T | snv | 1 | ||||
| rs387907352 | 1.000 | 7 | 2944529 | missense variant | C/T | snv | 1 |