ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.1548G>C (p.Pro516=) (rs143796254)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000465068 SCV000557591 likely benign not provided 2016-07-28 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000587776 SCV000697685 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV001418321 SCV001620546 likely benign MYH-associated polyposis 2016-07-26 criteria provided, single submitter clinical testing

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