| | | Single nucleotide variant (missense variant +1 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Deletion (frameshift variant +1 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Single nucleotide variant (splice acceptor variant) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Deletion (frameshift variant +1 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Duplication (frameshift variant +1 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Duplication | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Indel | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Insertion | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Insertion | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Single nucleotide variant (nonsense +2 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Single nucleotide variant (synonymous variant +2 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | Tubulointerstitial kidney disease, autosomal dominant, 2 | |
| | | Insertion | Tubulointerstitial kidney disease, autosomal dominant, 2 | |