ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.607-18_607-17del

dbSNP: rs765157527
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000480242 SCV000568112 likely benign not specified 2015-10-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV000580554 SCV000685658 likely benign Hereditary cancer-predisposing syndrome 2017-05-19 criteria provided, single submitter clinical testing
Mendelics RCV000708795 SCV000837765 likely benign Familial adenomatous polyposis 2 2018-07-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000708795 SCV002382617 likely benign Familial adenomatous polyposis 2 2023-11-22 criteria provided, single submitter clinical testing

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