ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.552T>C (p.Asn184=)

dbSNP: rs2100743257
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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 RCV002098530 SCV002399439 likely benign Immunodeficiency 37 2021-06-07 criteria provided, single submitter clinical testing

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