| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Duplication (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Deletion (frameshift variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (nonsense +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +2 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (stop lost) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) | |
| | | Single nucleotide variant (missense variant +1 more) | Peroxisome biogenesis disorder 11A (Zellweger) +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | PEX13-related disorder +3 more | |