| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | ANO3-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | ANO3-related disorder | |
| | | Single nucleotide variant (missense variant) | ANO3-related disorder +1 more | |
| | | Microsatellite (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Dystonic disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +3 more | |
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