| | | Single nucleotide variant (missense variant) | PEX12-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | PEX12-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Peroxisome biogenesis disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | PEX12-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder 3A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Peroxisome biogenesis disorder 3A (Zellweger) +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | PEX12-related disorder +1 more | |
| | | Single nucleotide variant (nonsense) | PEX12-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder 3A (Zellweger) +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder 3A (Zellweger) +1 more | |
| | | Single nucleotide variant (nonsense) | Peroxisome biogenesis disorder 3A (Zellweger) +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | PEX12-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | PEX12-related disorder | |