List of variants in gene PHACTR1 reported as likely pathogenic for neurodevelopmental 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_030948.6(PHACTR1):c.1278C>G (p.Ile426Met)
NM_030948.6(PHACTR1):c.190C>G (p.Arg64Gly)
NM_030948.6(PHACTR1):c.209C>G (p.Pro70Arg)

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