ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.433-10C>T

gnomAD frequency: 0.00004  dbSNP: rs371656670
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001403516 SCV001605388 likely benign Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2024-01-22 criteria provided, single submitter clinical testing

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