ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.333A>G (p.Leu111=)

dbSNP: rs763402710
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002159233 SCV002473489 likely benign Immunodeficiency 37 2023-06-04 criteria provided, single submitter clinical testing

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