"Baylor Genetics"[submitter] AND "WAS"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 11115	NM_000377.3(WAS):c.257G>A (p.Arg86His)	WAS (R86H)	Single nucleotide variant (missense variant)	not provided +3 more	GPathogenic
Select item 1030751	NM_000377.3(WAS):c.374G>A (p.Gly125Glu)	WAS (G125E)	Single nucleotide variant (missense variant)	Wiskott-Aldrich syndrome	GLikely pathogenic
Select item 625640	GRCh37/hg19 Xp11.3-11.23(chrX:43507300-48929622)	ARAF, CCDC120 +64 more	Copy number gain	not provided	GPathogenic

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