ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.942+19_942+29del

dbSNP: rs11309117
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002257140 SCV002526765 benign Hereditary cancer-predisposing syndrome 2020-01-02 criteria provided, single submitter curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465934 SCV002760637 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005558 SCV004819205 likely benign Lynch syndrome 2024-02-05 criteria provided, single submitter clinical testing

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