ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.445A>T (p.Asn149Tyr)

dbSNP: rs2147263992
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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 RCV002245339 SCV002515525 uncertain significance Wiskott-Aldrich syndrome no assertion criteria provided research

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