ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1076+171del

dbSNP: rs17217884
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001550441 SCV001770768 likely benign not provided 2019-08-07 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256818 SCV002528805 benign Hereditary cancer-predisposing syndrome 2021-05-01 criteria provided, single submitter curation

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