ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.2870-88T>C

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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 RCV003431194 SCV004149593 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing HDAC4: BS2

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