ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.942+14_942+29del

dbSNP: rs11309117
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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 RCV001262895 SCV001440931 benign Breast carcinoma 2019-01-01 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256726 SCV002526772 likely benign Hereditary cancer-predisposing syndrome 2020-11-18 criteria provided, single submitter curation

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