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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCP
(Q458H +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
GUncertain significance
VCP
(R191Q +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
+4 more
GPathogenic/Likely pathogenic