"Centogene AG - the Rare Disease Company"[submitter] AND "TBK1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333966	NM_013254.4(TBK1):c.94G>A (p.Gly32Ser)	TBK1 (G32S)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4	GUncertain significance
Select item 664607	NM_013254.4(TBK1):c.802A>G (p.Ser268Gly)	TBK1 (S268G)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 +1 more	GUncertain significance