List of variants in gene USP9X reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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.4603+19A>G	rs55900117	0.00771
NM_001039591.3(USP9X):c.6084C>T (p.Pro2028=)	rs146661515	0.00282
NM_001039591.3(USP9X):c.286G>T (p.Val96Leu)	rs73480414	0.00058

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