"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 287856	NM_000377.3(WAS):c.264C>T (p.Tyr88=)	WAS	Single nucleotide variant (synonymous variant)	WAS-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 36909	NM_000377.3(WAS):c.273+10_273+11dup	WAS	Duplication (intron variant)	X-linked severe congenital neutropenia +4 more	GBenign/Likely benign
Select item 135411	NM_000377.3(WAS):c.1378C>T (p.Pro460Ser)	WAS (P460S)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign

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