ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.942+16_942+29del

dbSNP: rs11309117
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581809 SCV000690144 benign Hereditary cancer-predisposing syndrome 2017-06-26 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000581809 SCV002526771 likely benign Hereditary cancer-predisposing syndrome 2021-01-31 criteria provided, single submitter curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320711 SCV004025233 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002337 SCV004824938 benign Lynch syndrome 2023-09-04 criteria provided, single submitter clinical testing

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