ClinVar Miner

Submissions for variant NM_001783.3(CD79A):c.419C>A (p.Thr140Asn) (rs148797987)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000120487 SCV000602945 uncertain significance not specified 2017-01-31 criteria provided, single submitter clinical testing
Invitae RCV000576287 SCV000676989 likely benign Agammaglobulinemia 3, autosomal recessive 2019-12-31 criteria provided, single submitter clinical testing
ITMI RCV000120487 SCV000084640 not provided not specified 2013-09-19 no assertion provided reference population

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