ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.850-16A>C

dbSNP: rs1557469033
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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 RCV000773741 SCV000907441 likely benign Hereditary cancer-predisposing syndrome 2018-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067273 SCV002349807 likely benign Familial adenomatous polyposis 2 2021-11-12 criteria provided, single submitter clinical testing

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