ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.705-7del

gnomAD frequency: 0.00001  dbSNP: rs1557472348
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000776963 SCV000912633 uncertain significance Hereditary cancer-predisposing syndrome 2018-12-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536713 SCV002982054 likely benign Familial adenomatous polyposis 2 2024-01-22 criteria provided, single submitter clinical testing

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