ClinVar Miner

Submissions for variant NM_015015.3(KDM4B):c.2793C>T (p.Asn931=)

gnomAD frequency: 0.00372  dbSNP: rs141629225
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000974483 SCV001122306 benign not provided 2018-07-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000974483 SCV002498403 benign not provided 2024-02-01 criteria provided, single submitter clinical testing KDM4B: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000974483 SCV005206542 likely benign not provided criteria provided, single submitter not provided

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