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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNB4
(V220M)
Single nucleotide variant
(missense variant +1 more)
Frontotemporal dementia
GLikely pathogenic
CHRNB4
(L60F)
Single nucleotide variant
(missense variant)
Frontotemporal dementia
GLikely pathogenic