"PreventionGenetics, part of Exact Sciences"[submitter] AND "NLGN2"[ge - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042506	NM_020795.4(NLGN2):c.457+10C>T	NLGN2	Single nucleotide variant (intron variant)	NLGN2-related condition	GLikely benign
Select item 3035647	NM_020795.4(NLGN2):c.1965C>G (p.Pro655=)	NLGN2	Single nucleotide variant (synonymous variant)	NLGN2-related condition	GLikely benign
Select item 3043717	NM_020795.4(NLGN2):c.2193C>T (p.Ala731=)	NLGN2	Single nucleotide variant (synonymous variant)	NLGN2-related condition	GLikely benign
Select item 3029306	NM_020795.4(NLGN2):c.2455G>T (p.Ala819Ser)	NLGN2 (A819S)	Single nucleotide variant (missense variant)	NLGN2-related condition	GLikely benign
Select item 3030315	NM_020795.4(NLGN2):c.2495C>T (p.Thr832Ile)	NLGN2 (T832I)	Single nucleotide variant (missense variant)	NLGN2-related condition	GUncertain significance

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