ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.492+15G>A

dbSNP: rs1557478098
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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 RCV000773591 SCV000907285 likely benign Hereditary cancer-predisposing syndrome 2018-07-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068507 SCV002339621 likely benign Familial adenomatous polyposis 2 2024-11-06 criteria provided, single submitter clinical testing

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