List of variants in gene USP9X reported as likely benign for brain disorder

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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_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.3797A>C (p.Lys1266Thr)	rs765979381
NM_001039591.3(USP9X):c.4060A>T (p.Ile1354Phe)	rs2519305704
NM_001039591.3(USP9X):c.4882C>A (p.Pro1628Thr)	rs2519335932
NM_001039591.3(USP9X):c.6434A>T (p.Gln2145Leu)

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