ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.687T>C (p.Thr229=)

gnomAD frequency: 0.00001  dbSNP: rs767413256
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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 RCV001480487 SCV001684804 likely benign Immunodeficiency 37 2023-10-13 criteria provided, single submitter clinical testing

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