ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.1359G>C (p.Gly453=)

dbSNP: rs35216603
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000916205 SCV001061438 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2025-01-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003432910 SCV004152595 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing DNMT3B: BP4, BP7

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