ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.159G>A (p.Leu53=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003784447 SCV004572807 likely benign X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome 2023-01-03 criteria provided, single submitter clinical testing

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