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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAPT
(A297V +1 more)
Single nucleotide variant
(missense variant +1 more)
Pick disease
+5 more
GUncertain significance
MAPT
(N279K +5 more)
Single nucleotide variant
(missense variant +1 more)
Frontotemporal dementia
+5 more
GPathogenic
MAPT
(P301L +5 more)
Single nucleotide variant
(missense variant +1 more)
Progressive supranuclear ophthalmoplegia
+5 more
GPathogenic
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