| | | Insertion (frameshift variant) | Primary hyperoxaluria type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Microsatellite (inframe_deletion) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary hyperoxaluria type 3 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary hyperoxaluria type 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (intron variant) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (intron variant) | Primary hyperoxaluria type 3 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Primary hyperoxaluria type 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (nonsense) | Primary hyperoxaluria type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Primary hyperoxaluria type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 | |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 +1 more | |
| | | Microsatellite (inframe_deletion) | Primary hyperoxaluria type 3 +2 more | |
| | | Single nucleotide variant (missense variant) | Primary hyperoxaluria type 3 +1 more | GConflicting classifications of pathogenicity |