ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1435-9T>C

dbSNP: rs372815910
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673832 SCV000799079 likely benign Familial adenomatous polyposis 2 2018-04-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000673832 SCV001626342 likely benign Familial adenomatous polyposis 2 2021-05-27 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584701 SCV004357792 likely benign Hereditary cancer-predisposing syndrome 2022-06-21 criteria provided, single submitter clinical testing

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