ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.347-5T>C

gnomAD frequency: 0.00770  dbSNP: rs77663629
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 RCV000531265 SCV000655454 benign Immunodeficiency 37 2024-01-29 criteria provided, single submitter clinical testing

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