ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1103-13C>T

dbSNP: rs781706856
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001190852 SCV001358445 likely benign Hereditary cancer-predisposing syndrome 2016-03-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560095 SCV003451184 likely benign Familial adenomatous polyposis 2 2023-12-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002560095 SCV004834826 likely benign Familial adenomatous polyposis 2 2023-10-06 criteria provided, single submitter clinical testing

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