ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1174C>T (p.Leu392=)

dbSNP: rs144079536
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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 RCV002155536 SCV002421225 likely benign Familial adenomatous polyposis 2 2022-11-14 criteria provided, single submitter clinical testing

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