| | | Single nucleotide variant (3 prime UTR variant +1 more) | ATP13A2-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | ATP13A2-related disorder +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Kufor-Rakeb syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | ATP13A2-related disorder | |
| | | Single nucleotide variant (missense variant) | Kufor-Rakeb syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A2-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Autosomal recessive spastic paraplegia type 78 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Kufor-Rakeb syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | ATP13A2-related disorder | |
| | | Single nucleotide variant (intron variant) | Kufor-Rakeb syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Kufor-Rakeb syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Kufor-Rakeb syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Kufor-Rakeb syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | ATP13A2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | ATP13A2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (intron variant) | ATP13A2-related disorder | |
| | | Single nucleotide variant (missense variant) | Kufor-Rakeb syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | ATP13A2-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive spastic paraplegia type 78 +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant) | Kufor-Rakeb syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Kufor-Rakeb syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | ATP13A2-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | Kufor-Rakeb syndrome +4 more | |
| | ATP13A2, LOC129929540 (A3P) | Single nucleotide variant (missense variant) | ATP13A2-related disorder +4 more | GConflicting classifications of pathogenicity |