ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.283C>T (p.Leu95=)

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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 RCV003080825 SCV003486826 likely benign X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome 2024-06-24 criteria provided, single submitter clinical testing

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