ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.157+30A>G (rs3219485)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000245935 SCV000306736 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001286858 SCV001473478 benign none provided 2020-03-30 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000245935 SCV000691952 benign not specified no assertion criteria provided clinical testing

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