ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.169C>G (p.His57Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV002280919 SCV002569093 likely pathogenic Familial adenomatous polyposis 2 2021-02-18 criteria provided, single submitter clinical testing

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