ClinVar Miner

Submissions for variant NM_000038.5(APC):c.2094A>G (p.Leu698=) (rs1426881729)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000646650 SCV000768425 likely benign Familial adenomatous polyposis 1 2017-11-30 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759419 SCV000888729 uncertain significance not provided 2017-09-25 criteria provided, single submitter clinical testing

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