ClinVar Miner

Submissions for variant NM_020661.4(AICDA):c.8+12G>T

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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 RCV002889483 SCV003233324 likely benign Hyper-IgM syndrome type 2 2022-12-08 criteria provided, single submitter clinical testing

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