ClinVar Miner

Submissions for variant NM_000038.6(APC):c.8033A>G (p.Asn2678Ser) (rs886059800)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000319284 SCV000452052 uncertain significance APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506899 SCV000600163 uncertain significance not specified 2017-03-20 criteria provided, single submitter clinical testing
Ambry Genetics RCV001027093 SCV001189596 uncertain significance Hereditary cancer-predisposing syndrome 2019-07-28 criteria provided, single submitter clinical testing Insufficient evidence

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