| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CLCNKA, LOC106501712 (A244V +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 4B +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | CLCNKA, LOC106501712 (D383Y +1 more) | Single nucleotide variant (missense variant) | Bartter disease type 4B | |
Click to view in NCBI Gene