ClinVar Miner

Submissions for variant NM_001127511.3(APC):c.166-29015A>T (rs75581138)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000602321 SCV000730394 benign not specified 2017-10-06 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.
Counsyl RCV000663007 SCV000786014 benign Familial adenomatous polyposis 1 2018-02-06 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000602321 SCV000859945 benign not specified 2018-06-07 criteria provided, single submitter clinical testing

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