ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.492+18G>A

gnomAD frequency: 0.00001  dbSNP: rs377647533
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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 RCV001185242 SCV001351414 uncertain significance Hereditary cancer-predisposing syndrome 2019-01-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003770061 SCV004687334 likely benign Familial adenomatous polyposis 2 2023-11-17 criteria provided, single submitter clinical testing

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