ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.360C>T (p.Ser120=)

gnomAD frequency: 0.00002  dbSNP: rs759056975
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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 RCV001451724 SCV001655365 likely benign Immunodeficiency 37 2024-12-09 criteria provided, single submitter clinical testing

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