ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5050T>C (p.Phe1684Leu) (rs886059795)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000280740 SCV000452020 uncertain significance APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000985305 SCV001133341 uncertain significance not provided 2018-11-29 criteria provided, single submitter clinical testing
Ambry Genetics RCV001023479 SCV001185365 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-31 criteria provided, single submitter clinical testing In silico models in agreement (benign);Insufficient evidence;Rarity in general population databases (dbsnp, esp, 1000 genomes)
Color RCV001023479 SCV001356947 uncertain significance Hereditary cancer-predisposing syndrome 2019-11-18 criteria provided, single submitter clinical testing

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