ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3647-2A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV004759490 SCV005368046 likely pathogenic Lynch syndrome 5 2024-05-08 criteria provided, single submitter clinical testing Criteria applied: PVS1,PM2_SUP

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