ClinVar Miner

Submissions for variant NM_000074.3(CD40LG):c.157-15G>C

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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 RCV002858640 SCV003234672 likely benign Hyper-IgM syndrome type 1 2022-08-27 criteria provided, single submitter clinical testing

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