ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.956-7C>T

dbSNP: rs778959035
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584567 SCV000691454 likely benign Hereditary cancer-predisposing syndrome 2016-11-17 criteria provided, single submitter clinical testing
Counsyl RCV000663316 SCV000786585 likely benign Generalized juvenile polyposis/juvenile polyposis coli 2018-05-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001495387 SCV001700069 likely benign Juvenile polyposis syndrome 2024-05-01 criteria provided, single submitter clinical testing

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