ClinVar Miner

Submissions for variant NM_001005273.3(CHD3):c.509+5G>A

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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 RCV004599119 SCV005092327 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing CHD3: BP4

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