| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LOC126862568, WNK4 (P313A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudohypoaldosteronism type 2B +1 more | |
| | LOC126862568, WNK4 (C59F +1 more) | Indel (missense variant) | Pseudohypoaldosteronism type 2B | |
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