ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1575A>G (p.Val525=)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002866436 SCV003227326 benign Hereditary nonpolyposis colorectal neoplasms 2022-08-06 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003585302 SCV004356690 likely benign Hereditary cancer-predisposing syndrome 2023-02-24 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007643 SCV004843838 likely benign Lynch syndrome 2023-11-20 criteria provided, single submitter clinical testing

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