"PreventionGenetics, part of Exact Sciences"[submitter] AND "VANGL2"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034367	NM_020335.3(VANGL2):c.12G>A (p.Glu4=)	VANGL2	Single nucleotide variant (synonymous variant)	VANGL2-related disorder	GLikely benign
Select item 708933	NM_020335.3(VANGL2):c.91C>T (p.Arg31Cys)	VANGL2 (R31C)	Single nucleotide variant (missense variant)	VANGL2-related disorder +1 more	GLikely benign
Select item 3041156	NM_020335.3(VANGL2):c.333G>A (p.Ala111=)	VANGL2	Single nucleotide variant (synonymous variant)	VANGL2-related disorder	GLikely benign
Select item 3050384	NM_020335.3(VANGL2):c.842A>G (p.His281Arg)	VANGL2 (H281R)	Single nucleotide variant (missense variant)	VANGL2-related disorder	GBenign
Select item 729599	NM_020335.3(VANGL2):c.1328C>T (p.Ala443Val)	VANGL2 (A443V)	Single nucleotide variant (missense variant)	VANGL2-related disorder +1 more	GBenign/Likely benign

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