ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.702C>G (p.Leu234=)

dbSNP: rs863224699
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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 RCV002200597 SCV002482201 likely benign Familial adenomatous polyposis 2 2020-12-20 criteria provided, single submitter clinical testing

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