ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.378+16G>C

dbSNP: rs1004284031
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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 RCV000773360 SCV000907054 likely benign Hereditary cancer-predisposing syndrome 2018-06-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002534058 SCV003339308 likely benign Familial adenomatous polyposis 2 2022-04-08 criteria provided, single submitter clinical testing

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