ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1365C>G (p.Thr455=)

dbSNP: rs150269172
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001494337 SCV001698990 likely benign Familial adenomatous polyposis 2 2020-08-06 criteria provided, single submitter clinical testing

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