ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1095C>G (p.Pro365=)

dbSNP: rs1570380575
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001422507 SCV001625058 likely benign Familial adenomatous polyposis 2 2018-04-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001422507 SCV004834065 likely benign Familial adenomatous polyposis 2 2023-07-19 criteria provided, single submitter clinical testing

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