ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.1447+10C>G

dbSNP: rs2144474920
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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 RCV001409989 SCV001612030 likely benign Juvenile polyposis syndrome 2020-09-11 criteria provided, single submitter clinical testing

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