| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (splice donor variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +5 more | |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +4 more | |
| | | Single nucleotide variant (synonymous variant) | Infantile neuroaxonal dystrophy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive Parkinson disease 14 +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | PLA2G6-associated neurodegeneration +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive Parkinson disease 14 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive Parkinson disease 14 | |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (nonsense) | not provided +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | PLA2G6-related disorder +11 more | GConflicting classifications of pathogenicity |