ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.346+9T>C

dbSNP: rs538273638
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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 RCV000979231 SCV001127170 benign Immunodeficiency 37 2023-12-02 criteria provided, single submitter clinical testing

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