ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.1661+17T>G (rs377461923)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000582515 SCV000690007 benign Hereditary cancer-predisposing syndrome 2015-12-02 criteria provided, single submitter clinical testing
Counsyl RCV000663193 SCV000786368 likely benign Lynch syndrome I 2018-04-18 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679294 SCV000806006 benign not specified 2017-08-24 criteria provided, single submitter clinical testing

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