ClinVar Miner

Submissions for variant NM_001375834.1(WIPF1):c.182-10T>C

dbSNP: rs1013513013
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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 RCV001429681 SCV001632398 likely benign Wiskott-Aldrich syndrome 2 2024-10-16 criteria provided, single submitter clinical testing

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