ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.379-10G>A

dbSNP: rs1553129380
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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 RCV000777101 SCV000912787 likely benign Hereditary cancer-predisposing syndrome 2017-12-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001458732 SCV001662559 likely benign Familial adenomatous polyposis 2 2024-03-06 criteria provided, single submitter clinical testing

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