ClinVar Miner

Submissions for variant NM_001367624.2(ZNF469):c.114C>T (p.Asn38=)

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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 RCV003673133 SCV004393806 likely benign not provided 2022-11-16 criteria provided, single submitter clinical testing

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