ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.1371G>A (p.Gly457=) (rs1553125186)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000780499 SCV000917804 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV001437095 SCV001639941 likely benign MYH-associated polyposis 2020-09-24 criteria provided, single submitter clinical testing

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