"Diagnostic Laboratory, Strasbourg University Hospital"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 978847	NM_181303.2(NLGN3):c.163C>G (p.Arg55Gly)	NLGN3 (R55G)	Single nucleotide variant (missense variant +1 more)	Intellectual disability	GUncertain significance
Select item 235850	NM_181303.2(NLGN3):c.1849C>T (p.Arg617Trp)	NLGN3 (R597W +3 more)	Single nucleotide variant (missense variant)	Intellectual disability	GLikely pathogenic