ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.606+21C>A (rs148552450)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986304 SCV001135261 benign MYH-associated polyposis 2019-05-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000429 SCV001157243 benign not specified 2018-09-23 criteria provided, single submitter clinical testing
Invitae RCV000986304 SCV001718973 benign MYH-associated polyposis 2020-12-04 criteria provided, single submitter clinical testing
GeneDx RCV001538427 SCV001756077 likely benign not provided 2018-06-21 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27829682)

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