ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5802C>G (p.Pro1934=) (rs876658810)

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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 RCV000220324 SCV000274530 likely benign Hereditary cancer-predisposing syndrome 2015-03-11 criteria provided, single submitter clinical testing
GeneDx RCV000432312 SCV000527153 likely benign not specified 2016-04-26 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000471656 SCV000562575 likely benign Familial adenomatous polyposis 1 2016-12-04 criteria provided, single submitter clinical testing
Color RCV000220324 SCV000687047 likely benign Hereditary cancer-predisposing syndrome 2017-11-06 criteria provided, single submitter clinical testing

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