| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | ATP13A3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (intron variant) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (intron variant) | ATP13A3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | ATP13A3-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Duplication (intron variant) | ATP13A3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | ATP13A3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | ATP13A3-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |