ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.822G>A (p.Val274=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003506561 SCV004296091 likely benign Familial adenomatous polyposis 2 2023-07-03 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584120 SCV004358578 likely benign Hereditary cancer-predisposing syndrome 2017-04-04 criteria provided, single submitter clinical testing

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