"Centogene AG - the Rare Disease Company"[submitter] AND "USP9X"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1307353	NM_001039591.3(USP9X):c.904G>A (p.Ala302Thr)	USP9X (A302T)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 99 +1 more	GUncertain significance
Select item 1333756	NM_001039591.3(USP9X):c.7431+243G>A	USP9X	Single nucleotide variant (intron variant)	Intellectual disability, X-linked 99	GUncertain significance