ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.465C>T (p.Gly155=)

dbSNP: rs1645187281
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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 RCV001183374 SCV001349090 likely benign Hereditary cancer-predisposing syndrome 2019-06-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559835 SCV003226044 likely benign Familial adenomatous polyposis 2 2022-10-31 criteria provided, single submitter clinical testing

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