ClinVar Miner

Submissions for variant NM_005869.4(CWC27):c.938+3212_938+3213dup

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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 RCV004811649 SCV005431732 benign not provided 2024-11-01 criteria provided, single submitter clinical testing CWC27: BS1, BS2

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