ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.933C>T (p.Cys311=)

dbSNP: rs1323382632
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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 RCV001182880 SCV001348479 likely benign Hereditary cancer-predisposing syndrome 2019-07-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001416826 SCV001619015 likely benign Familial adenomatous polyposis 2 2019-10-28 criteria provided, single submitter clinical testing

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