ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.2727G>C (p.Glu909Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV005257460 SCV005909611 likely benign not provided 2025-03-01 criteria provided, single submitter clinical testing ZNF292: BP4

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