ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.360+5G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV003314538 SCV004014034 uncertain significance Wiskott-Aldrich syndrome criteria provided, single submitter clinical testing

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