List of variants in gene USP9X reported as likely benign for Intellectual disability, X-linked 99; Intellectual disability, X-linked 99, syndromic, female-restricted

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_001039591.3(USP9X):c.3028-7A>G	rs115310559	0.00480
NM_001039591.3(USP9X):c.6360A>G (p.Ile2120Met)	rs201128029	0.00014
NM_001039591.3(USP9X):c.4882C>A (p.Pro1628Thr)	rs2519335932

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