| | | Duplication (frameshift variant) | Fanconi renotubular syndrome 2 | |
| | | Duplication (frameshift variant) | Fanconi renotubular syndrome 2 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypercalcemia, infantile, 2 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hypercalcemia, infantile, 2 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Deletion (inframe_deletion) | Hypercalcemia, infantile, 2 +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi renotubular syndrome 2 | |
| | | Single nucleotide variant (intron variant) | Fanconi renotubular syndrome 2 +1 more | GConflicting classifications of pathogenicity |
| | | Copy number loss | Hypercalcemia, infantile, 2 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (missense variant) | SLC34A1-related condition +4 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi renotubular syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (nonsense) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hypercalcemia, infantile, 2 +3 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi renotubular syndrome 2 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hypercalcemia, infantile, 2 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (nonsense) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +4 more | |
| | | Single nucleotide variant (intron variant) | Hypophosphatemic nephrolithiasis/osteoporosis 1 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Deletion (inframe_deletion) | Hypercalcemia, infantile, 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Hypercalcemia, infantile, 2 +2 more | |
| | | Duplication (inframe_insertion) | not provided | |