"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 929068	NM_181303.2(NLGN3):c.26C>T (p.Ser9Leu)	NLGN3 (S9L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 918125	NM_181303.2(NLGN3):c.38G>A (p.Ser13Asn)	NLGN3 (S13N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2691361	NM_181303.2(NLGN3):c.237C>G (p.Ile79Met)	NLGN3 (I79M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1698659	NM_181303.2(NLGN3):c.1429C>G (p.Leu477Val)	NLGN3 (L340V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2581232	NM_181303.2(NLGN3):c.2194C>T (p.Arg732Cys)	NLGN3 (R595C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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