ClinVar Miner

Submissions for variant NM_005359.5(SMAD4):c.84A>G (p.Gln28=) (rs778465458)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000572232 SCV000671969 likely benign Hereditary cancer-predisposing syndrome 2015-02-04 criteria provided, single submitter clinical testing
Color RCV000572232 SCV000691439 likely benign Hereditary cancer-predisposing syndrome 2017-05-22 criteria provided, single submitter clinical testing
Invitae RCV000555128 SCV000632808 likely benign Juvenile polyposis syndrome 2017-12-20 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679592 SCV000806705 likely benign not provided 2017-11-21 criteria provided, single submitter clinical testing

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