| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CLCNKB, LOC106501713 (R76*) | Single nucleotide variant (nonsense) | not provided +3 more | |
| | CLCNKB, LOC106501713 (V207fs) | Deletion (frameshift variant) | Bartter disease type 3 | |
Click to view in NCBI Gene