| | | Single nucleotide variant (missense variant +1 more) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (nonsense +1 more) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant +1 more) | Infantile neuroaxonal dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (nonsense) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant) | Neurodegeneration with brain iron accumulation 2B +3 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant +1 more) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive Parkinson disease 14 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +3 more | |
| | | Single nucleotide variant (nonsense) | Neurodegeneration with brain iron accumulation 2B +1 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (splice donor variant) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Deletion (intron variant) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +5 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive Parkinson disease 14 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Neurodegeneration with brain iron accumulation 2B | |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Infantile neuroaxonal dystrophy +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) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | PLA2G6-associated neurodegeneration +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive Parkinson disease 14 +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +4 more | GConflicting classifications of pathogenicity |
| | | Duplication (inframe_insertion) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Infantile neuroaxonal dystrophy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Infantile osteopetrosis with neuroaxonal dysplasia +9 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 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PLA2G6-associated neurodegeneration +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | PLA2G6-associated neurodegeneration +4 more | |
| | | 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) | Infantile neuroaxonal dystrophy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PLA2G6-associated neurodegeneration +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (nonsense) | PLA2G6-associated neurodegeneration +6 more | GPathogenic/Likely pathogenic |
| | | Deletion (inframe_deletion) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | PLA2G6-related condition +11 more | GConflicting classifications of pathogenicity |