ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.-6-9_-6-8del

dbSNP: rs1557493461
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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 RCV001425771 SCV001628409 likely benign Familial adenomatous polyposis 2 2019-03-25 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001425771 SCV004825265 likely benign Familial adenomatous polyposis 2 2023-08-15 criteria provided, single submitter clinical testing

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