ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.492+19G>A

dbSNP: rs1241875704
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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 RCV000583541 SCV000690586 likely benign Hereditary cancer-predisposing syndrome 2017-04-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002529266 SCV003475015 likely benign Familial adenomatous polyposis 2 2024-01-15 criteria provided, single submitter clinical testing

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