List of variants in gene NLGN1 reported as uncertain significance for Autism, susceptibility to, 20

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365925.2(NLGN1):c.2532G>A (p.Ter844=)	rs568763160	0.00004
NM_001365925.2(NLGN1):c.278G>A (p.Arg93His)	rs749776633	0.00003
NM_001365925.2(NLGN1):c.1634C>T (p.Pro545Leu)	rs752889815	0.00001
NM_001365925.2(NLGN1):c.493+5G>A

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