ClinVar Miner

Submissions for variant NM_000074.3(CD40LG):c.289-19G>T

dbSNP: rs2148552369
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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 RCV002146339 SCV002468936 likely benign Hyper-IgM syndrome type 1 2023-11-19 criteria provided, single submitter clinical testing

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