"PreventionGenetics, part of Exact Sciences"[submitter] AND "CLEC7A"[g - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718877	NM_197947.3(CLEC7A):c.739A>T (p.Met247Leu)	CLEC7A (M168L +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GLikely benign
Select item 4466	NM_197947.3(CLEC7A):c.714T>G (p.Tyr238Ter)	CLEC7A (Y238* +2 more)	Single nucleotide variant (nonsense +2 more)	CLEC7A-related condition +3 more	GBenign/Likely benign
Select item 3035819	NM_197947.3(CLEC7A):c.493-10T>C	CLEC7A	Single nucleotide variant (intron variant)	CLEC7A-related condition	GLikely benign
Select item 3042662	NM_197947.3(CLEC7A):c.340+9A>G	CLEC7A	Single nucleotide variant (intron variant)	CLEC7A-related condition	GLikely benign

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