ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1539A>G (p.Ala513=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV002481147 SCV002774652 uncertain significance not provided 2021-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003614198 SCV004447470 likely benign Familial adenomatous polyposis 2 2023-03-20 criteria provided, single submitter clinical testing

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