List of variants in gene NLGN3 reported as uncertain significance for Autism, susceptibility to, X-linked 1

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_181303.2(NLGN3):c.1384G>A (p.Ala462Thr)	rs2519768091
NM_181303.2(NLGN3):c.163C>T (p.Arg55Ter)	rs759137635
NM_181303.2(NLGN3):c.1685C>T (p.Thr562Ile)
NM_181303.2(NLGN3):c.2342A>G (p.His781Arg)
NM_181303.2(NLGN3):c.707A>G (p.Asn236Ser)	rs2092405042
NM_181303.2(NLGN3):c.806G>A (p.Ser269Asn)	rs2092439435

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