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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APP
(A200V +3 more)
Single nucleotide variant
(missense variant)
Cerebral amyloid angiopathy, APP-related
+1 more
GConflicting classifications of pathogenicity
APP
Single nucleotide variant
(intron variant)
Early-onset autosomal dominant Alzheimer disease
+1 more
GUncertain significance