ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2551_2552insTTATA (p.Ser851fs)

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Total submissions: 2
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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 RCV002468857 SCV002765039 likely pathogenic Lynch syndrome 5 2022-12-15 criteria provided, single submitter clinical testing _x000D_ Criteria applied: PVS1, PM2_SUP
CeGaT Center for Human Genetics Tuebingen RCV003326634 SCV004033732 pathogenic not provided 2023-07-01 criteria provided, single submitter clinical testing MSH6: PVS1, PM2

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