ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.453A>G (p.Thr151=)

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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 RCV003093450 SCV003471006 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2023-12-25 criteria provided, single submitter clinical testing

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