ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.606+18C>T

dbSNP: rs1557475530
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001177737 SCV001342000 likely benign Hereditary cancer-predisposing syndrome 2019-01-30 criteria provided, single submitter clinical testing
Invitae RCV002555478 SCV003513506 likely benign Familial adenomatous polyposis 2 2023-06-09 criteria provided, single submitter clinical testing

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