ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.1308+11A>C

dbSNP: rs773719398
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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 RCV000583452 SCV000691396 likely benign Hereditary cancer-predisposing syndrome 2017-03-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061939 SCV002411095 likely benign Juvenile polyposis syndrome 2024-02-05 criteria provided, single submitter clinical testing

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