ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.420+18G>A

dbSNP: rs1645216268
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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 RCV001186093 SCV001352437 likely benign Hereditary cancer-predisposing syndrome 2018-11-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001463006 SCV001666936 likely benign Familial adenomatous polyposis 2 2024-01-08 criteria provided, single submitter clinical testing

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