ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1277-3127A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003327029 SCV004033724 likely benign not provided 2025-02-01 criteria provided, single submitter clinical testing MSH2: BS1

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