ClinVar Miner

Submissions for variant NM_000038.6(APC):c.8013T>C (p.Ser2671=) (rs1294217069)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000570627 SCV000667492 likely benign Hereditary cancer-predisposing syndrome 2016-02-11 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000646572 SCV000768346 likely benign Familial adenomatous polyposis 1 2017-11-13 criteria provided, single submitter clinical testing

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