ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.58-3dup

dbSNP: rs754835118
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 RCV002136721 SCV002410217 benign Immunodeficiency 37 2024-05-24 criteria provided, single submitter clinical testing

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