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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PSEN1
(K307R +1 more)
Single nucleotide variant
(missense variant)
Alzheimer disease 3
+5 more
GUncertain significance
MAPT
Single nucleotide variant
(intron variant)
Frontotemporal dementia
GLikely benign