"NIHR Bioresource Rare Diseases, University of Cambridge"[submitter] A - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 11123	NM_000377.3(WAS):c.134C>T (p.Thr45Met)	WAS (T45M)	Single nucleotide variant (missense variant)	Thrombocytopenia +4 more	GConflicting classifications of pathogenicity
Select item 627275	NM_000377.3(WAS):c.217T>A (p.Cys73Ser)	WAS (C73S)	Single nucleotide variant (missense variant)	Thrombocytopenia	GUncertain significance