| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Copy number loss | Bartter disease type 4A | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (synonymous variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (synonymous variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Bartter disease type 4A +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (3 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (3 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (splice donor variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Deletion (frameshift variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Deletion (frameshift variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (nonsense) | Bartter disease type 4A +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Bartter disease type 4A +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (5 prime UTR variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Bartter disease type 4A +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Bartter disease type 4A | |
| | | Single nucleotide variant (missense variant) | Bartter syndrome +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Bartter disease type 4A +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice acceptor variant +1 more) | Bartter disease type 4A | |
| | | Deletion (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Bartter syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |