ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.793-10dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, Hannover Medical School RCV004577415 SCV005061446 uncertain significance Familial adenomatous polyposis 4 2024-06-18 criteria provided, single submitter clinical testing

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