ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.1086C>T (p.Ala362=) (rs878854182)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000230115 SCV000285915 likely benign MYH-associated polyposis 2020-12-03 criteria provided, single submitter clinical testing
Ambry Genetics RCV001017167 SCV001178203 likely benign Hereditary cancer-predisposing syndrome 2018-07-16 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Color Health, Inc RCV001017167 SCV001342805 likely benign Hereditary cancer-predisposing syndrome 2018-11-29 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001526928 SCV001737691 likely benign not specified 2021-05-22 criteria provided, single submitter clinical testing

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