ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.942+22_942+29del

dbSNP: rs11309117
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986657 SCV001135712 benign Lynch syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Leipzig Medical Center RCV001262883 SCV001440918 likely benign Breast carcinoma 2019-01-01 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255600 SCV002526767 benign Hereditary cancer-predisposing syndrome 2020-12-12 criteria provided, single submitter curation
Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C. RCV002255600 SCV004014923 likely benign Hereditary cancer-predisposing syndrome 2023-03-09 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493765 SCV004243549 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing

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