ClinVar Miner

Submissions for variant NM_020661.4(AICDA):c.428-5del

dbSNP: rs5796316
Minimum review status: Collection method:
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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 RCV001411289 SCV001613348 likely benign Hyper-IgM syndrome type 2 2024-11-14 criteria provided, single submitter clinical testing

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