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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRN
(N119del)
Microsatellite
(inframe_deletion)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
+2 more
GUncertain significance
GRN, LOC125177489
Single nucleotide variant
(splice acceptor variant)
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
GPathogenic