| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | GNMT, PEX6 (R860W +1 more) | Microsatellite (3 prime UTR variant +2 more) | Peroxisome biogenesis disorder 4B | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Microsatellite (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Insertion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +2 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Indel (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Microsatellite (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Indel (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Indel (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Heimler syndrome 2 +1 more | |
| | | Deletion (frameshift variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder | |
| | | Deletion (frameshift variant +1 more) | Heimler syndrome 2 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 4A (Zellweger) +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Heimler syndrome 2 +3 more | |
| | | Single nucleotide variant (intron variant +1 more) | Heimler syndrome 2 +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 4B +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Heimler syndrome 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Heimler syndrome 2 +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +2 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PEX6-related disorder +2 more | |
| | | Insertion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) | |
| | | Indel (frameshift variant +1 more) | Heimler syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Heimler syndrome 2 +3 more | |
| | | Microsatellite (inframe_deletion +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice donor variant) | Peroxisome biogenesis disorder +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | Peroxisome biogenesis disorder +2 more | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +3 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant +1 more) | Heimler syndrome 2 +2 more | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Duplication (frameshift variant +1 more) | Heimler syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Heimler syndrome 2 +2 more | |
| | | Microsatellite (frameshift variant +1 more) | Peroxisome biogenesis disorder +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +2 more) | Heimler syndrome 2 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Microsatellite (frameshift variant +1 more) | Heimler syndrome 2 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (splice donor variant) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder 4A (Zellweger) +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant) | Peroxisome biogenesis disorder +2 more | |
| | | Duplication (frameshift variant +1 more) | Heimler syndrome 2 +2 more | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder +4 more | GPathogenic/Likely pathogenic |
| | | Duplication (inframe_insertion +1 more) | Peroxisome biogenesis disorder +2 more | |
| | | Deletion (inframe_deletion +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |
| | | Microsatellite (inframe_deletion +1 more) | Peroxisome biogenesis disorder 4A (Zellweger) +1 more | |