List of variants in gene NRXN1 reported as pathogenic for Autism spectrum disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.1066del (p.Glu356fs)
NM_001330078.2(NRXN1):c.3430C>T (p.Arg1144Ter)	rs1282230077
NM_001330078.2(NRXN1):c.471dup (p.Leu158fs)

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