ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.205T>C (p.Leu69=)

gnomAD frequency: 0.00006  dbSNP: rs745539994
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001461807 SCV001665715 likely benign Immunodeficiency 37 2023-10-10 criteria provided, single submitter clinical testing

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