ClinVar Miner

Submissions for variant NM_000074.3(CD40LG):c.156+17G>A

gnomAD frequency: 0.00001  dbSNP: rs755782893
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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 RCV001519876 SCV001728836 benign Hyper-IgM syndrome type 1 2023-12-01 criteria provided, single submitter clinical testing

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