ClinVar Miner

Submissions for variant NM_000074.2(CD40LG):c.38C>T (p.Ala13Val) (rs368003929)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000726000 SCV000341139 uncertain significance not provided 2016-05-18 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000339805 SCV000602944 uncertain significance not specified 2017-02-23 criteria provided, single submitter clinical testing
Invitae RCV001089061 SCV001043078 benign X-linked hyper-IgM syndrome 2019-12-31 criteria provided, single submitter clinical testing

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