ClinVar Miner

Submissions for variant NM_005632.3(CAPN15):c.1842+4G>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 RCV003395102 SCV004131690 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing CAPN15: BP4

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