ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1392+10T>A

dbSNP: rs2149110334
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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 RCV001444937 SCV001647955 likely benign Familial adenomatous polyposis 2 2020-12-23 criteria provided, single submitter clinical testing

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