ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.914-5C>T

dbSNP: rs786203632
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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 RCV000640403 SCV000761994 likely benign Familial adenomatous polyposis 2 2017-10-29 criteria provided, single submitter clinical testing

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