ClinVar Miner

Submissions for variant NM_001367624.2(ZNF469):c.11826C>G (p.Gly3942=)

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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 RCV003691452 SCV004425780 likely benign not provided 2023-01-08 criteria provided, single submitter clinical testing

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