ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.849+7C>T

gnomAD frequency: 0.00002  dbSNP: rs775005184
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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 RCV001186083 SCV001352426 uncertain significance Hereditary cancer-predisposing syndrome 2019-06-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001428339 SCV001631036 likely benign Familial adenomatous polyposis 2 2024-12-04 criteria provided, single submitter clinical testing

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