ClinVar Miner

Submissions for variant NM_020661.4(AICDA):c.428-17_428-16dup

dbSNP: rs5796316
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001844124 SCV000381280 uncertain significance Hyperimmunoglobulin M syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000960058 SCV001107005 benign Hyper-IgM syndrome type 2 2024-01-02 criteria provided, single submitter clinical testing
GeneDx RCV001548092 SCV001767945 likely benign not provided 2019-09-20 criteria provided, single submitter clinical testing

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