ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.1059A>C (p.Pro353=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003438238 SCV004166224 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing WAS: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003778455 SCV004571655 likely benign X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome 2023-12-19 criteria provided, single submitter clinical testing

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