C1833296[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333969	NM_014043.4(CHMP2B):c.421A>G (p.Met141Val)	CHMP2B (M100V +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	GUncertain significance
Select item 1333970	NM_014043.4(CHMP2B):c.423G>A (p.Met141Ile)	CHMP2B (M100I +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	GUncertain significance