"VAMP2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040494	NM_014232.3(VAMP2):c.183G>A (p.Ser61=)	VAMP2	Single nucleotide variant (synonymous variant)	VAMP2-related condition	GLikely benign
Select item 3052949	NM_014232.3(VAMP2):c.147C>T (p.Asn49=)	VAMP2	Single nucleotide variant (synonymous variant)	VAMP2-related condition	GLikely benign
Select item 2229982	NM_014232.3(VAMP2):c.124-3C>T	VAMP2	Single nucleotide variant (intron variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 3030387	NM_014232.3(VAMP2):c.65C>T (p.Pro22Leu)	LOC130060218, VAMP2 (P22L +1 more)	Single nucleotide variant (missense variant)	VAMP2-related condition	GUncertain significance

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