ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.513A>G (p.Thr171=)

dbSNP: rs2145949316
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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 RCV002129106 SCV002459814 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2021-12-09 criteria provided, single submitter clinical testing

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