ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1277-7C>G

dbSNP: rs375437307
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001696782 SCV000535305 likely benign not provided 2019-07-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000944077 SCV001090039 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-04-10 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001190853 SCV001358446 likely benign Hereditary cancer-predisposing syndrome 2018-04-24 criteria provided, single submitter clinical testing

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