ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.477G>A (p.Pro159=)

gnomAD frequency: 0.00001  dbSNP: rs375939126
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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 RCV002139753 SCV002445496 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2024-10-24 criteria provided, single submitter clinical testing

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