ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.304+13_304+15del

dbSNP: rs1645306069
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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 RCV001184891 SCV001350979 likely benign Hereditary cancer-predisposing syndrome 2019-04-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068399 SCV002394512 likely benign Familial adenomatous polyposis 2 2024-12-02 criteria provided, single submitter clinical testing

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