ClinVar Miner

Submissions for variant NM_005359.6(SMAD4):c.1473T>C (p.Gly491=)

dbSNP: rs1207826883
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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 RCV000583643 SCV000691402 likely benign Hereditary cancer-predisposing syndrome 2017-10-12 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000780718 SCV000918226 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV001460937 SCV001664820 likely benign Juvenile polyposis syndrome 2023-04-30 criteria provided, single submitter clinical testing

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