| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC106501712, CLCNKA (E586* +2 more) | Single nucleotide variant (nonsense) | Bartter disease type 4B | |
| | CLCNKA, LOC106501712 (V657M +2 more) | Single nucleotide variant (missense variant) | Bartter disease type 4B +1 more | |
Click to view in NCBI Gene