ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.2334G>C (p.Ser778=)

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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 RCV005118448 SCV005743841 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2024-02-19 criteria provided, single submitter clinical testing

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