| | LOC126862568, WNK4 (E271V) | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | LOC126862568, WNK4 (P274L) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (S281N) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (K387R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC126862568, WNK4 (M1L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC126862568, WNK4 (R275Q) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC126862568, WNK4 (R329L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126862568, WNK4 (C364G +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126862568, WNK4 (G320E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Pseudohypoaldosteronism type 2B | |
| | | Single nucleotide variant (missense variant) | Pseudohypoaldosteronism type 2B | |
| | | Single nucleotide variant (nonsense) | Pseudohypoaldosteronism type 2B | |
| | LOC126862568, WNK4 (R20S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (V295G) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (T314I) | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (P345S) | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases | |
| | LOC126862568, WNK4 (R301G) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC126862568, WNK4 (R294fs) | Deletion (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Pseudohypoaldosteronism type 2B | |
| | WNK4, LOC126862568 (C52S +1 more) | Single nucleotide variant (missense variant) | Pseudohypoaldosteronism type 2B | |
| | LOC126862568, WNK4 (P313A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | LOC126862568, WNK4 (C59F +1 more) | Indel (missense variant) | Pseudohypoaldosteronism type 2B | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudohypoaldosteronism type 2B +1 more | |
| | LOC126862568, WNK4 (A325T +1 more) | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |