ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.379-11T>C

gnomAD frequency: 0.00001  dbSNP: rs1645235855
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003614696 SCV004449816 likely benign Familial adenomatous polyposis 2 2024-06-04 criteria provided, single submitter clinical testing

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