ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.1272T>C (p.Asp424=)

dbSNP: rs2144452726
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002137682 SCV002415088 likely benign Juvenile polyposis syndrome 2022-01-26 criteria provided, single submitter clinical testing

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