ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3150T>C (p.Ala1050=)

dbSNP: rs776990271
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002269196 SCV002552320 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004808242 SCV005429388 likely benign Lynch syndrome 2024-07-10 criteria provided, single submitter clinical testing

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