| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cerebral amyloid angiopathy, APP-related +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Early-onset autosomal dominant Alzheimer disease +1 more | |
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