| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CLCNKB, LOC106501713 (A206S) | Single nucleotide variant (missense variant) | Bartter disease type 4B +1 more | |
| | CLCNKB, LOC106501713 (G289R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC106501713, CLCNKB (G464A +1 more) | Single nucleotide variant (missense variant) | not provided | |
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