ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.42T>A (p.Thr14=)

dbSNP: rs1570341297
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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 RCV001482914 SCV001687293 likely benign Immunodeficiency 37 2018-12-09 criteria provided, single submitter clinical testing

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