ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3919_3920insGAT (p.Asn1307delinsArgTyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004013949 SCV004840099 uncertain significance Lynch syndrome 2024-01-12 criteria provided, single submitter clinical testing

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