ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.1655A>C (p.His552Pro)

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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 RCV004579665 SCV005062160 uncertain significance Lynch syndrome 5 2024-06-28 criteria provided, single submitter clinical testing

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