| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion | BARTTER SYNDROME, TYPE 4B, WITH SENSORINEURAL DEAFNESS | |
| | CLCNKA, LOC106501712 (W80C) | Single nucleotide variant (missense variant +1 more) | Bartter disease type 4B | |
Click to view in NCBI Gene